Found: 13
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Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.
- Published in:
- Human Genetics, 2000, v. 107, n. 1, p. 7, doi. 10.1007/s004390050002
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- Publication type:
- Article
Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 2, p. 255, doi. 10.1038/sj.ejhg.5200273
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- Publication type:
- Article
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNA<sup>Ser(UCN)</sup> gene.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 1, p. 45, doi. 10.1038/sj.ejhg.5200247
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- Publication type:
- Article
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
- Published in:
- Nature Genetics, 2005, v. 37, n. 3, p. 289, doi. 10.1038/ng1514
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- Publication type:
- Article
Acoustic Hearing After Murine Cochlear Implantation.
- Published in:
- Annals of Otology, Rhinology & Laryngology, 2015, v. 124, n. 12, p. 931, doi. 10.1177/0003489415592162
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- Publication type:
- Article
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment.
- Published in:
- 1999
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- Publication type:
- Erratum
Device Design Modifications Informed by In Vitro Testing of Bacterial Attachment Reduce Infection Rates of Cochlear Implants in Clinical Practice.
- Published in:
- Microorganisms, 2021, v. 9, n. 9, p. 1, doi. 10.3390/microorganisms9091809
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- Publication type:
- Article
Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3.
- Published in:
- Journal of the Peripheral Nervous System, 2002, v. 7, n. 2, p. 87, doi. 10.1046/j.1529-8027.2002.02014.x
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- Publication type:
- Article
Perilymph pharmacokinetics of marker applied through a cochlear implant in guinea pigs.
- Published in:
- PLoS ONE, 2017, v. 12, n. 8, p. 1, doi. 10.1371/journal.pone.0183374
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- Publication type:
- Article
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.
- Published in:
- Brain: A Journal of Neurology, 2009, v. 132, n. 7, p. 1741, doi. 10.1093/brain/awp115
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- Publication type:
- Article
A deafness mutation isolates a second role for the tectorial membrane in hearing.
- Published in:
- Nature Neuroscience, 2005, v. 8, n. 8, p. 1035, doi. 10.1038/nn1496
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- Publication type:
- Article
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2.
- Published in:
- Annals of Neurology, 2006, v. 59, n. 2, p. 276
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- Publication type:
- Article
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 3, p. 195, doi. 10.1093/hmg/10.3.195
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- Publication type:
- Article