A missense mutation in CRYGD linked with autosomal dominant congenital cataract of aculeiform type.
about
Crystal structure of the cataract-causing P23T γD-crystallin mutantTargeted Exome Sequencing of Congenital Cataracts Related Genes: Broadening the Mutation Spectrum and Genotype-Phenotype Correlations in 27 Chinese Han Families.A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataractInherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.Interstitial deletion at chromosome 16p13.2 involving TMEM114 (transmembrane protein 114) in a boy and his father without cataract.
P2860
A missense mutation in CRYGD linked with autosomal dominant congenital cataract of aculeiform type.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
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2012年學術文章
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2012年學術文章
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name
A missense mutation in CRYGD l ...... l cataract of aculeiform type.
@en
A missense mutation in CRYGD l ...... l cataract of aculeiform type.
@nl
type
label
A missense mutation in CRYGD l ...... l cataract of aculeiform type.
@en
A missense mutation in CRYGD l ...... l cataract of aculeiform type.
@nl
prefLabel
A missense mutation in CRYGD l ...... l cataract of aculeiform type.
@en
A missense mutation in CRYGD l ...... l cataract of aculeiform type.
@nl
P2860
P1476
A missense mutation in CRYGD l ...... l cataract of aculeiform type.
@en
P2093
Daljit Singh
Vanita Vanita
P2860
P2888
P304
P356
10.1007/S11010-012-1355-2
P577
2012-06-06T00:00:00Z