Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.

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Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Simultaneous multi‑gene mutati ...... impairment in Northwest China.

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Simultaneous multi‑gene mutati ...... impairment in Northwest China.

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type

Item

label

Simultaneous multi‑gene mutati ...... impairment in Northwest China.

@en

Simultaneous multi‑gene mutati ...... impairment in Northwest China.

@nl

prefLabel

Simultaneous multi‑gene mutati ...... impairment in Northwest China.

@en

Simultaneous multi‑gene mutati ...... impairment in Northwest China.

@nl

P1476

Simultaneous multi‑gene mutati ...... impairment in Northwest China.

@en

P2093

Jian-Li Ma

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Shi-Hong Duan

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Xiao-Long Yang

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Yu-Fen Guo

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P2860

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

Connexin-26 mutations in sporadic and inherited sensorineural deafness

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations

GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review

Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

Different matrilineal contributions to genetic structure of ethnic groups in the silk road region in china.

Hereditary deafness and phenotyping in humans.

The p.V37I exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment.

P304

6722-6728

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P31

scholarly article

P356

10.3892/MMR.2017.7431

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P433

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P478

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P577

2017-09-07T00:00:00Z

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P698

28901477

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P932

5865789

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