reference/5961824

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5961824

Outgoing Links

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endingPage	423
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publicationName	Annals of Human Genetics
startingPage	410
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bibliographicCitation	Cheng J, Zhou X, Lu Y, Chen J, Han B, Zhu Y, Liu L, Choy K, Han D, Sham PC, Zhang MQ, Zhang X, Yuan H. Exome Sequencing Identifies a Novel Frameshift Mutation ofMYO6as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family. Annals of Human Genetics. 2014 Sep 17;78(6):410–23. doi: 10.1111/ahg.12084.
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date	2014-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1111/ahg.12084 https://pubmed.ncbi.nlm.nih.gov/25227905
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Exome Sequencing Identifies a Novel Frameshift Mutation ofMYO6as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family
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