Title: Albinism in a patient with mutations at both the <scp>OA</scp>1 and <scp>OCA</scp>3 loci
Abstract: Pigment Cell & Melanoma ResearchVolume 29, Issue 1 p. 107-109 Letter to the Editor Albinism in a patient with mutations at both the OA1 and OCA3 loci Fanny Morice-Picard, Fanny Morice-Picard Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, University Bordeaux, Bordeaux, France CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceThese authors contributed equally to the work.Search for more papers by this authorEulalie Lasseaux, Eulalie Lasseaux CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceThese authors contributed equally to the work.Search for more papers by this authorClaudio Plaisant, Claudio Plaisant CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorDorothée Cailley, Dorothée Cailley CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorJulie Bouron, Julie Bouron CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorCaroline Rooryck, Caroline Rooryck Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, University Bordeaux, Bordeaux, France CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorDidier Lacombe, Didier Lacombe Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, University Bordeaux, Bordeaux, France CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorValérie Pelletier, Valérie Pelletier Centre de référence pour les Affections Rares en Génétique Ophtalmologique (CARGO), Hôpital Civil, Strasbourg, France Service de Génétique Médicale, Hôpital de Hautepierre, Strasbourg, FranceSearch for more papers by this authorDan Lipsker, Dan Lipsker Service de Dermatologie, Hôpital Civil, Strasbourg, FranceSearch for more papers by this authorYaumara Perdomo-Trujillo, Yaumara Perdomo-Trujillo Centre de référence pour les Affections Rares en Génétique Ophtalmologique (CARGO), Hôpital Civil, Strasbourg, France Service de Génétique Médicale, Hôpital de Hautepierre, Strasbourg, FranceSearch for more papers by this authorHélène Dollfus, Hélène Dollfus Centre de référence pour les Affections Rares en Génétique Ophtalmologique (CARGO), Hôpital Civil, Strasbourg, France Service de Génétique Médicale, Hôpital de Hautepierre, Strasbourg, France Laboratoire de Génétique Médicale, INSERM U1112, Strasbourg, FranceSearch for more papers by this authorBenoit Arveiler, Corresponding Author Benoit Arveiler Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, University Bordeaux, Bordeaux, France CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceCorrespondence Pr. Benoît Arveiler, e-mail: [email protected]Search for more papers by this author Fanny Morice-Picard, Fanny Morice-Picard Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, University Bordeaux, Bordeaux, France CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceThese authors contributed equally to the work.Search for more papers by this authorEulalie Lasseaux, Eulalie Lasseaux CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceThese authors contributed equally to the work.Search for more papers by this authorClaudio Plaisant, Claudio Plaisant CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorDorothée Cailley, Dorothée Cailley CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorJulie Bouron, Julie Bouron CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorCaroline Rooryck, Caroline Rooryck Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, University Bordeaux, Bordeaux, France CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorDidier Lacombe, Didier Lacombe Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, University Bordeaux, Bordeaux, France CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceSearch for more papers by this authorValérie Pelletier, Valérie Pelletier Centre de référence pour les Affections Rares en Génétique Ophtalmologique (CARGO), Hôpital Civil, Strasbourg, France Service de Génétique Médicale, Hôpital de Hautepierre, Strasbourg, FranceSearch for more papers by this authorDan Lipsker, Dan Lipsker Service de Dermatologie, Hôpital Civil, Strasbourg, FranceSearch for more papers by this authorYaumara Perdomo-Trujillo, Yaumara Perdomo-Trujillo Centre de référence pour les Affections Rares en Génétique Ophtalmologique (CARGO), Hôpital Civil, Strasbourg, France Service de Génétique Médicale, Hôpital de Hautepierre, Strasbourg, FranceSearch for more papers by this authorHélène Dollfus, Hélène Dollfus Centre de référence pour les Affections Rares en Génétique Ophtalmologique (CARGO), Hôpital Civil, Strasbourg, France Service de Génétique Médicale, Hôpital de Hautepierre, Strasbourg, France Laboratoire de Génétique Médicale, INSERM U1112, Strasbourg, FranceSearch for more papers by this authorBenoit Arveiler, Corresponding Author Benoit Arveiler Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, University Bordeaux, Bordeaux, France CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, FranceCorrespondence Pr. Benoît Arveiler, e-mail: [email protected]Search for more papers by this author First published: 06 August 2015 https://doi.org/10.1111/pcmr.12408Citations: 3 Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References Chiang, P.-W., Spector, E., and Tsai, A.C.-H. (2009). Oculocutaneous albinism spectrum. Am. J. Med. Genet. A 149A, 1590–1591. Fairbank, P.D., Lee, C., Ellis, A., Hildebrand, J.D., Gross, J.M., and Wallingford, J.B. (2006). 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Genet. A 164, 1268–1271. Tijmes, N.T., Bergen, A.B., and De Jong, P.T. (1998). Paucity of signs in X linked ocular albinism with a 700 kb deletion spanning the OA1 gene. Br. J. Ophthalmol. 82, 457–458. Citing Literature Volume29, Issue1January 2016Pages 107-109 ReferencesRelatedInformation