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Uncommon mutation in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
David, Jasna; Okiro, Julie Omolola; Murphy, Kevin; Elamin, Marwa.
Affiliation
  • David J; Department of Neurology, Sligo University Hospital, Sligo, Ireland.
  • Okiro JO; Department of Medicine, Sligo University Hospital, Sligo, Ireland.
  • Murphy K; Department of Neurology, Sligo University Hospital, Sligo, Ireland.
  • Elamin M; Department of Neurology, Sligo University Hospital, Sligo, Ireland.
BMJ Case Rep ; 20172017 Feb 27.
Article in En | MEDLINE | ID: mdl-28242802
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / MELAS Syndrome / Mitochondrial Proteins / Electron Transport Complex I Limits: Adult / Humans / Male Language: En Journal: BMJ Case Rep Year: 2017 Type: Article Affiliation country: Ireland
Fulltext
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / MELAS Syndrome / Mitochondrial Proteins / Electron Transport Complex I Limits: Adult / Humans / Male Language: En Journal: BMJ Case Rep Year: 2017 Type: Article Affiliation country: Ireland