PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p

Benzer Materyaller

• Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
  Yazar:: Tamura, Shigehiko, ve diğerleri
  Baskı/Yayın Bilgisi: (1998)
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  Yazar:: Otera, Hidenori, ve diğerleri
  Baskı/Yayın Bilgisi: (1998)
• A newly identified mutation in the PEX26 gene is associated with a milder form of Zellweger spectrum disorder
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  Baskı/Yayın Bilgisi: (2019)
• The Peroxin Pex3p Initiates Membrane Assembly in Peroxisome Biogenesis
  Yazar:: Ghaedi, Kamran, ve diğerleri
  Baskı/Yayın Bilgisi: (2000)
• Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
  Yazar:: Matsuzono, Yuji, ve diğerleri
  Baskı/Yayın Bilgisi: (1999)