reference/14680030

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14680030

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endingPage	498
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pageRange	493-498
publicationName	The American Journal of Human Genetics
startingPage	493
bibliographicCitation	Hanein S, Perrault I, Roche O, Gerber S, Khadom N, Rio M, Boddaert N, Jean-Pierre M, Brahimi N, Serre V, Chretien D, Delphin N, Fares-Taie L, Lachheb S, Rotig A, Meire F, Munnich A, Dufier J, Kaplan J, Rozet J. TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy. The American Journal of Human Genetics. 2009 Apr;84(4):493–8. doi: 10.1016/j.ajhg.2009.03.003.
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date	200904
identifier	https://pubmed.ncbi.nlm.nih.gov/19327736 https://pubmed.ncbi.nlm.nih.gov/PMC2667974 https://doi.org/10.1016/j.ajhg.2009.03.003
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy
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