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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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
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N Kinoshita
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S Tamura
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N Shimozawa
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M Hamasaki
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K Ghaedi
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R J Wanders
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Y Suzuki
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N Kondo
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Y Fujiki
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2 March 1999
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96
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5
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2116-21
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