Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I

The peroxisome biogenesis disorders (PBDs), including Zellweger syndrome (ZS) and neonatal adrenoleukodystrophy (NALD), are autosomal recessive diseases caused by defects in peroxisome assembly, for which at least 10 complementation groups have been reported. We have isolated a human PEX1 cDNA (HsPE...

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Hlavní autoři: Tamura, Shigehiko, Okumoto, Kanji, Toyama, Ryusuke, Shimozawa, Nobuyuki, Tsukamoto, Toshiro, Suzuki, Yasuyuki, Osumi, Takashi, Kondo, Naomi, Fujiki, Yukio
Médium: Artigo
Jazyk:Inglês
Vydáno: The National Academy of Sciences 1998
Témata:
Biological Sciences
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC22492/
https://ncbi.nlm.nih.gov/pubmed/9539740
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