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Article

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

Science (New York, N.Y.) - 29 May 1998

Wang A, Liang Y, Fridell R A, Probst F J, Wilcox E R, Touchman J W, Morton C C, Morell R J, Noben-Trauth K, Camper S A, Friedman T B

Abstract excerpt

DFNB3, a locus for nonsyndromic sensorineural recessive deafness, maps to a 3-centimorgan interval on human chromosome 17p11.2, a region that shows conserved synteny with mouse shaker-2. A human unconventional myosin gene, MYO15, was identified by combining functional and positional cloning appro...

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Identifiers

PMID: 9603736
DOI: 10.1126/science.280.5368.1447

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-9603736-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.PMID 9603736Read ↗

Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.Semantic proximity Read ↗

Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus.Semantic proximity Read ↗

Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.Semantic proximity Read ↗

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.Semantic proximity Read ↗

Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A.Semantic proximity Read ↗

MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.Semantic proximity Read ↗

Association of a novel missense mutation in MYO15A with nonsyndromic hearing loss: a case reportSemantic proximity Read ↗

Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss.Semantic proximity Read ↗

Identification of novel compound heterozygous mutations of the MYO15A gene with autosomal recessive non-syndromic hearing loss.Semantic proximity Read ↗

Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.Semantic proximity Read ↗

Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing loss.Semantic proximity Read ↗

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