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PubMed (cited) for id: 618246
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Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
J Med Genet. 2012 Apr;49(4):277-83. doi: 10.1136/jmedgenet-2012-100846.
J Med Genet. 2012.
PMID: 22499348
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.
Calvo SE, Compton AG, Hershman SG, Lim SC, Lieber DS, Tucker EJ, Laskowski A, Garone C, Liu S, Jaffe DB, Christodoulou J, Fletcher JM, Bruno DL, Goldblatt J, Dimauro S, Thorburn DR, Mootha VK.
Calvo SE, et al.
Sci Transl Med. 2012 Jan 25;4(118):118ra10. doi: 10.1126/scitranslmed.3003310.
Sci Transl Med. 2012.
PMID: 22277967
Free PMC article.
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