Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly (Q22008838)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly |
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Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly (English)
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Y Matsuzono
N Kinoshita
S Tamura
N Shimozawa
M Hamasaki
K Ghaedi
R J Wanders
Y Suzuki
N Kondo
Y Fujiki
2 March 1999
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96
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2116-21
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5
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1 reference
1 reference