Open AccessBenign Cox Deficiency Myopathy
Author(s) -
J Gordon Millichap
Publication year - 2011
Publication title -
pediatric neurology briefs
Language(s) - Uncategorized
Resource type - Journals
eISSN - 2166-6482
pISSN - 1043-3155
DOI - 10.15844/pedneurbriefs-25-2-6
Subject(s) - neurology , pathological , myopathy , medicine , cytochrome c oxidase , pediatrics , mitochondrial myopathy , mitochondrial disease , leigh disease , pathology , psychiatry , mitochondrion , biology , mutation , mitochondrial dna , genetics , gene