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PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G

Peroxisome biogenesis disorders (PBDs) such as Zellweger syndrome (ZS) and neonatal adrenoleukodystrophy are autosomal recessive diseases caused by defects in peroxisome assembly, for which 13 genotypes have been identified. Expression of the human peroxin Pex3p cDNA encoding a 373-amino-acid peroxi...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Ghaedi, Kamran, Honsho, Masanori, Shimozawa, Nobuyuki, Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: The American Society of Human Genetics 2000
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1287899/
https://ncbi.nlm.nih.gov/pubmed/10968777
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