reference/29482975

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/29482975

Outgoing Links

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contentType	Comparative Study\|Journal Article\|Research Support, N.I.H., Extramural\|Research Support, Non-U.S. Gov't
endingPage	152
issn	0002-9297
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pageRange	144-152
publicationName	The American Journal of Human Genetics
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bibliographicCitation	Shahin H, Walsh T, Sobe T, Abu Sa’ed J, Abu Rayan A, Lynch ED, Lee MK, Avraham KB, King M, Kanaan M. Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss. The American Journal of Human Genetics. 2006 Jan;78(1):144–52. doi: 10.1086/499495.
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date	200601
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC1380212 https://pubmed.ncbi.nlm.nih.gov/16385458 https://doi.org/10.1086/499495
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss
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Total number of triples: 65.