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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...

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Bibliografske podrobnosti
Main Authors: Ghaedi, Kamran, Honsho, Masanori, Shimozawa, Nobuyuki, Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Format: Artigo
Jezik:Inglês
Izdano: The American Society of Human Genetics 2000
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1287899/
https://ncbi.nlm.nih.gov/pubmed/10968777
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