reference/7334039

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contentType	Journal Article
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pageRange	627-631
publicationName	The American Journal of Human Genetics
startingPage	627
bibliographicCitation	Nota B, Struys E, Pop A, Jansen E, Fernandez Ojeda M, Kanhai W, Kranendijk M, van Dooren SM, Bevova M, Sistermans E, Nieuwint AM, Barth M, Ben-Omran T, Hoffmann G, de Lonlay P, McDonald M, Meberg A, Muntau A, Nuoffer J, Parini R, Read M, Renneberg A, Santer R, Strahleck T, van Schaftingen E, van der Knaap M, Jakobs C, Salomons G. Deficiency in SLC25A1, Encoding the Mitochondrial Citrate Carrier, Causes Combined D-2- and L-2-Hydroxyglutaric Aciduria. The American Journal of Human Genetics. 2013 Apr;92(4):627–31. doi: 10.1016/j.ajhg.2013.03.009.
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date	2013-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1016/j.ajhg.2013.03.009 https://pubmed.ncbi.nlm.nih.gov/23561848 https://pubmed.ncbi.nlm.nih.gov/PMC3617390
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Deficiency in SLC25A1, Encoding the Mitochondrial Citrate Carrier, Causes Combined D-2- and L-2-Hydroxyglutaric Aciduria
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