reference/2522253

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2522253

Outgoing Links

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contentType	Journal Article
endingPage	556
issn	0165-5876
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pageRange	553-556
publicationName	International Journal of Pediatric Otorhinolaryngology
startingPage	553
bibliographicCitation	Keivani A, Haghighat-Nia A, Fazel-Najafabadi E, Hosseinzadeh M, Salehi M. A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family. International Journal of Pediatric Otorhinolaryngology. 2015 Apr;79(4):553–6. doi: 10.1016/j.ijporl.2015.01.027.
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date	201504
identifier	https://doi.org/10.1016/j.ijporl.2015.01.027 https://pubmed.ncbi.nlm.nih.gov/25708704
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family
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Incoming Links

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Total number of triples: 44.