A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family.
about
Chemical inhibition of prometastatic lysyl-tRNA synthetase-laminin receptor interaction.Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing lossMolecular investigation of pediatric portuguese patients with sensorineural hearing loss.
P2860
A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family.
description
2009 nî lūn-bûn
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2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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name
A novel missense mutation p.L7 ...... eafness in a Brazilian family.
@en
A novel missense mutation p.L7 ...... eafness in a Brazilian family.
@nl
type
label
A novel missense mutation p.L7 ...... eafness in a Brazilian family.
@en
A novel missense mutation p.L7 ...... eafness in a Brazilian family.
@nl
prefLabel
A novel missense mutation p.L7 ...... eafness in a Brazilian family.
@en
A novel missense mutation p.L7 ...... eafness in a Brazilian family.
@nl
P2093
P2860
P1476
A novel missense mutation p.L7 ...... deafness in a Brazilian family
@en
P2093
A C Batissoco
A Tabith-Junior
M T B M Auricchio
P2860
P304
P356
10.1590/S0100-879X2009000200004
P407
P577
2009-02-01T00:00:00Z