Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation.

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Bibliographic Details
Title: Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation.
Authors: Demarest ST; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA., Whitehead MT; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA., Turnacioglu S; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA., Pearl PL; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA., Gropman AL; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA AGropman@childrensnational.org.
Source: Journal of child neurology [J Child Neurol] 2014 Sep; Vol. 29 (9), pp. 1249-56. Date of Electronic Publication: 2014 Jul 17.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Sage Country of Publication: United States NLM ID: 8606714 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1708-8283 (Electronic) Linking ISSN: 08830738 NLM ISO Abbreviation: J Child Neurol Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1708-8283
DOI:10.1177/0883073814538511