about
Identifcation of a novel mutation p.I240T in the FRMD7 gene in a family with congenital nystagmus.The clinical evaluation of infantile nystagmus: What to do first and why.Oculomotor neurocircuitry, a structural connectivity study of infantile nystagmus syndrome.A start codon mutation of the FRMD7 gene in two Korean families with idiopathic infantile nystagmus.A FRMD7 variant in a Japanese family causes congenital nystagmusMolecular genetic analysis of patients with sporadic and X-linked infantile nystagmusExpression and localization of Inter-alpha Inhibitors in rodent brain.Abnormally Small Neuromuscular Junctions in the Extraocular Muscles From Subjects With Idiopathic Nystagmus and Nystagmus Associated With Albinism.A novel missense mutation in the FERM domain containing 7 (FRMD7) gene causing X-linked idiopathic congenital nystagmus in a Chinese familyIdentification of three novel mutations in the FRMD7 gene for X-linked idiopathic congenital nystagmus.A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus.Novel mutations of FRMD7 in Chinese patients with congenital motor nystagmus.Structural analyses of FERM domain-mediated membrane localization of FARP1.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
The Role of FRMD7 in Idiopathic Infantile Nystagmus.
@en
type
label
The Role of FRMD7 in Idiopathic Infantile Nystagmus.
@en
prefLabel
The Role of FRMD7 in Idiopathic Infantile Nystagmus.
@en
P2093
P2860
P356
P1476
The Role of FRMD7 in Idiopathic Infantile Nystagmus.
@en
P2093
Chris J Talbot
Rachel J Watkins
Sue Shackleton
P2860
P304
P356
10.1155/2012/460956
P577
2011-08-29T00:00:00Z