Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.

MATSUZONO Y; KINOSHITA N; TAMURA S; SHIMOZAWA N; HAMASAKI M; GHAEDI K; WANDERS R J A; SUZUKI Y; FUJIKI Y

Art

J-GLOBAL ID：200902124449147092 Reference number：99A0431877

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.

ヒトPEX19 機能的相補によるcDNAクローニング,Zellweger症候群患者での変異解析とペルオキシソームと膜会合での推定役割

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Material：
Volume： 96 Issue： 5 Page： 2116-2121 Publication year： Mar. 02, 1999
JST Material Number： D0387A ISSN： 0027-8424 Document type： Article
Article type：原著論文 Country of issue： United States (USA) Language： ENGLISH (EN)

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