Novel ALDH3A2 Heterozygous Mutations in a Japanese Family with Sjögren–Larsson Syndrome-Reference-Cited by-同舟云学术

Novel ALDH3A2 Heterozygous Mutations in a Japanese Family with Sjögren–Larsson Syndrome

Published:2006-11 Issue:11 Volume:126 Page:2545-2547
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Sakai Kaori,Akiyama Masashi,Watanabe Tomoyuki,Sanayama Kazunori,Sugita Katsuo,Takahashi Mari,Suehiro Keisuke,Yorifuji Kazuhiko,Shibaki Akihiko,Shimizu Hiroshi

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

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4. Sjögren–Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene;De Laurenzi;Nat Genet,1996

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