Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.
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Genetics of vestibular disorders: pathophysiological insightsA New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing.Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueductEfficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians.Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueductMutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, ChinaThe genetic bases for non-syndromic hearing loss among ChineseMolecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan AssayHypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct.Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.Genetic diagnosis and cochlear implantation for patients with nonsyndromic hearing loss and enlarged vestibular aqueduct.Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss.Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.Screening of SLC26A4, FOXI1, KCNJ10, and GJB2 in bilateral deafness patients with inner ear malformation.A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss.GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.
P2860
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P2860
Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
Molecular analysis of hearing ...... que SLC26A4 mutation spectrum.
@en
Molecular analysis of hearing ...... que SLC26A4 mutation spectrum.
@nl
type
label
Molecular analysis of hearing ...... que SLC26A4 mutation spectrum.
@en
Molecular analysis of hearing ...... que SLC26A4 mutation spectrum.
@nl
prefLabel
Molecular analysis of hearing ...... que SLC26A4 mutation spectrum.
@en
Molecular analysis of hearing ...... que SLC26A4 mutation spectrum.
@nl
P2093
P1476
Molecular analysis of hearing ...... que SLC26A4 mutation spectrum.
@en
P2093
Desheng Liang
Heping Dai
Jiahui Xia
Lingqian Wu
Norio Niikawa
P2888
P304
P356
10.1007/S10038-007-0139-0
P577
2007-04-19T00:00:00Z