Title: Human erythropoietic protoporphyria: identification of a mutation at the splice donor site of intron 7 causing exon 7 skipping of the ferrochelatase gene
Abstract: Journal Article Human erythropoietic protoporphyria: identification of a mutation at the splice donor site of intron 7 causing exon 7 skipping of the ferrochelatase gene Get access Yoshitsugu Nakahashi, Yoshitsugu Nakahashi * *To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Hiroaki Miyazaki, Hiroaki Miyazaki Search for other works by this author on: Oxford Academic PubMed Google Scholar Yoichi Kadota, Yoichi Kadota Search for other works by this author on: Oxford Academic PubMed Google Scholar Yuji Naitoh, Yuji Naitoh Search for other works by this author on: Oxford Academic PubMed Google Scholar Kyoichi Inoue, Kyoichi Inoue Search for other works by this author on: Oxford Academic PubMed Google Scholar Masayuki Yamamoto, Masayuki Yamamoto 2Department of Biochemistry, Tohoku University School of MedicineSendai 980, Japan Search for other works by this author on: Oxford Academic PubMed Google Scholar Norio Hayashi, Norio Hayashi 2Department of Biochemistry, Tohoku University School of MedicineSendai 980, Japan Search for other works by this author on: Oxford Academic PubMed Google Scholar Shigeru Taketani Shigeru Taketani 1Department of Hygiene, Kansai Medical UniversityMoriguchi, Osaka 570, Japan Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 2, Issue 7, July 1993, Pages 1069–1070, https://doi.org/10.1093/hmg/2.7.1069 Published: 01 July 1993 Article history Received: 01 March 1993 Revision received: 22 April 1993 Accepted: 22 April 1993 Published: 01 July 1993
Publication Year: 1993
Publication Date: 1993-01-01
Language: en
Type: article
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 35
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