Population haplotypes of exon ORF15 of the retinitis pigmentosa GTPase regulator gene in Germany : implications for screening for inherited retinal disorders.
about
Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families.Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa.Loss of RPGR glutamylation underlies the pathogenic mechanism of retinal dystrophy caused by TTLL5 mutations
P2860
Population haplotypes of exon ORF15 of the retinitis pigmentosa GTPase regulator gene in Germany : implications for screening for inherited retinal disorders.
description
2006 nî lūn-bûn
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2006年の論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
@zh-tw
2006年论文
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name
Population haplotypes of exon ...... r inherited retinal disorders.
@en
Population haplotypes of exon ...... r inherited retinal disorders.
@nl
type
label
Population haplotypes of exon ...... r inherited retinal disorders.
@en
Population haplotypes of exon ...... r inherited retinal disorders.
@nl
prefLabel
Population haplotypes of exon ...... r inherited retinal disorders.
@en
Population haplotypes of exon ...... r inherited retinal disorders.
@nl
P2093
P2860
P356
P1476
Population haplotypes of exon ...... r inherited retinal disorders.
@en
P2093
Carsten M Pusch
Daniela Karra
Felix K Jacobi
Martina Broghammer
Nikolaus Blin
P2860
P2888
P304
P356
10.1007/BF03256451
P577
2006-01-01T00:00:00Z