Non-syndromic hereditary sensorineural hearing loss: review of the genes involved.
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Genetics of Nonsyndromic Congenital Hearing LossCharacterization of ATPase Activity of P2RX2 Cation ChannelHOMER2, a stereociliary scaffolding protein, is essential for normal hearing in humans and mice.Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese FamilyDifferent Phenotypes of the Two Chinese Probands with the Same c.889G>A (p.C162Y) Mutation in COCH Gene Verify Different Mechanisms Underlying Autosomal Dominant Nonsyndromic Deafness 9.Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in KoreansDevelopment of the stria vascularis and potassium regulation in the human fetal cochlea: Insights into hereditary sensorineural hearing lossOver-expression of myosin7A in cochlear hair cells of circling mice.Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.
P2860
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P2860
Non-syndromic hereditary sensorineural hearing loss: review of the genes involved.
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article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Non-syndromic hereditary sensorineural hearing loss: review of the genes involved.
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type
label
Non-syndromic hereditary sensorineural hearing loss: review of the genes involved.
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prefLabel
Non-syndromic hereditary sensorineural hearing loss: review of the genes involved.
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P2860
P1476
Non-syndromic hereditary sensorineural hearing loss: review of the genes involved.
@en
P2093
P2860
P356
10.1017/S0022215113003265
P577
2014-01-14T00:00:00Z