reference/16163588

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16163588

Outgoing Links

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contentType	Case Reports\|Journal Article
issn	1469-5073 0016-6723
pageRange	e10-
publicationName	Genetics Research
startingPage	e10
bibliographicCitation	Cohen L, Tzur S, Goldenberg-Cohen N, Bormans C, Behar DM, Reinstein E. Exome sequencing identified a novel de novo OPA1 mutation in a consanguineous family presenting with optic atrophy. Genet Res (Camb). 2016 Jun 06;98():e10. PMID: 27265430; PMCID: PMC6865152.
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date	2016-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC6865152 https://pubmed.ncbi.nlm.nih.gov/27265430 https://doi.org/10.1017/s0016672316000070
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Exome sequencing identified a novelde novo OPA1mutation in a consanguineous family presenting with optic atrophy
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Total number of triples: 49.