Title: Novel mutations in <i><scp>PCYT1A</scp></i> are responsible for spondylometaphyseal dysplasia with cone‐rod dystrophy
Abstract: Clinical GeneticsVolume 85, Issue 6 p. 532-533 HOTSPOTS Novel mutations in PCYT1A are responsible for spondylometaphyseal dysplasia with cone-rod dystrophy C.K. Wong, C.K. Wong [email protected] Department of Medical Genetics, Child and Family Research Institute, Vancouver, British Columbia, CanadaSearch for more papers by this author C.K. Wong, C.K. Wong [email protected] Department of Medical Genetics, Child and Family Research Institute, Vancouver, British Columbia, CanadaSearch for more papers by this author First published: 29 January 2014 https://doi.org/10.1111/cge.12353Citations: 3 e-mail: [email protected] 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 No abstract is available for this article.Citing Literature Volume85, Issue6June 2014Pages 532-533 RelatedInformation
Publication Year: 2014
Publication Date: 2014-02-24
Language: en
Type: letter
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 3
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