reference/26693977

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26693977

Outgoing Links

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endingPage	366
issn	1460-2083
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pageRange	361-366
publicationName	Human Molecular Genetics
startingPage	361
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bibliographicCitation	de Kok YJ, Bom SJ, Brunt TM, Kemperman MH, van Beusekom E, van der Velde-Visser SD, Robertson NG, Morton CC, Huygen PL, Verhagen WI, Brunner HG, Cremers CW, Cremers FP. A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects. Hum Mol Genet. 1999 Feb;8(2):361–6. doi: 10.1093/hmg/8.2.361. PMID: 9931344.
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date	1999-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1093/hmg/8.2.361 https://pubmed.ncbi.nlm.nih.gov/9931344
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects
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