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Article

A commentary on 'TECTA mutations in Japanese with mid-frequency hearing loss affected by Zona Pellucida domain protein secretion'.

Journal of human genetics - 1 Oct 2012

Maeda Yukihide, Fukushima Kunihiro

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22875146
DOI: 10.1038/jhg.2012.89

Genes

TECTA

Provenance

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Related research

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A commentary on 'TECTA mutations in Japanese with mid-frequency hearing loss affected by Zona Pellucida domain protein secretion'.PMID 22875146Read ↗

TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion.Semantic proximity Read ↗

Novel TECTA mutations identified in stable sensorineural hearing loss and their clinical implications.Semantic proximity Read ↗

Splice-altering variant in TECTA as a cause of hearing loss DFNA8/12Semantic proximity Read ↗

[From gene to disease; DFNA8/12, an autosomal dominant inherited bowl-shaped sensorineural hearing impairment].Semantic proximity Read ↗

Clinical relevance of the TECTA c.6183G>T variant identified in a family with autosomal dominant hearing loss: a case report.Semantic proximity Read ↗

Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNASemantic proximity Read ↗

<i>TECTB</i> Variants Reveal Tectorial Membrane Vulnerability in Dominant Non-Syndromic Hearing LossSemantic proximity Read ↗

A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation.Semantic proximity Read ↗

Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families.Semantic proximity Read ↗

Flat threshold and mid-frequency hearing impairment in a Dutch DFNA8/12 family with a novel mutation in TECTA. Some evidence for protection of the inner ear.Semantic proximity Read ↗

Association of Clinical Features With Mutation of TECTA in a Family With Autosomal Dominant Hearing LossSemantic proximity Read ↗

Ultrarare missense and frameshift variants in the <i>TECTA</i> gene may involve tectorial membrane in familial Meniere diseaseSemantic proximity Read ↗

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