The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypes.
about
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group GPEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum Disorder.
P2860
The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypes.
description
2000 nî lūn-bûn
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2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած
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2000 թվականի փետրվարին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
The human PEX3 gene encoding a ...... lysis in candidate phenotypes.
@ast
The human PEX3 gene encoding a ...... lysis in candidate phenotypes.
@en
type
label
The human PEX3 gene encoding a ...... lysis in candidate phenotypes.
@ast
The human PEX3 gene encoding a ...... lysis in candidate phenotypes.
@en
prefLabel
The human PEX3 gene encoding a ...... lysis in candidate phenotypes.
@ast
The human PEX3 gene encoding a ...... lysis in candidate phenotypes.
@en
P2093
P356
P1476
The human PEX3 gene encoding a ...... lysis in candidate phenotypes.
@en
P2093
Holzinger A
Kammerer S
Mayerhofer PU
Roscher AA
P304
P356
10.1006/BBRC.2000.2193
P407
P577
2000-02-01T00:00:00Z