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Mitochondrial DNA mutation "m.3243A>G"-Heterogeneous clinical picture for cardiologists ("m.3243A>G": A phenotypic chameleon).
Niedermayr, Katharina; Pölzl, Gerhard; Scholl-Bürgi, Sabine; Fauth, Christine; Schweigmann, Ulrich; Haberlandt, Edda; Albrecht, Ursula; Zlamy, Manuela; Sperl, Wolfgang; Mayr, Johannes A; Karall, Daniela.
Affiliation
  • Niedermayr K; Department of Child and Adolescent Health, Pediatrics I/III, Medical University of Innsbruck, Innsbruck, Austria.
  • Pölzl G; University Hospital for Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Innsbruck, Austria.
  • Scholl-Bürgi S; Department of Child and Adolescent Health, Pediatrics I/III, Medical University of Innsbruck, Innsbruck, Austria.
  • Fauth C; Department of Medical Genetics, Molecular and Clinical Pharmacology, Human Genetics Division, Medical University of Innsbruck, Innsbruck, Austria.
  • Schweigmann U; Department of Child and Adolescent Health, Pediatrics I/III, Medical University of Innsbruck, Innsbruck, Austria.
  • Haberlandt E; Department of Child and Adolescent Health, Pediatrics I/III, Medical University of Innsbruck, Innsbruck, Austria.
  • Albrecht U; Department of Child and Adolescent Health, Pediatrics I/III, Medical University of Innsbruck, Innsbruck, Austria.
  • Zlamy M; Department of Child and Adolescent Health, Pediatrics I/III, Medical University of Innsbruck, Innsbruck, Austria.
  • Sperl W; University Children's Hospital, Paracelsus Medical University Salzburg, Salzburg, Austria.
  • Mayr JA; University Children's Hospital, Paracelsus Medical University Salzburg, Salzburg, Austria.
  • Karall D; Department of Child and Adolescent Health, Pediatrics I/III, Medical University of Innsbruck, Innsbruck, Austria.
Congenit Heart Dis ; 13(5): 671-677, 2018 Sep.
Article in En | MEDLINE | ID: mdl-30133155
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / MELAS Syndrome / Heart Ventricles / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: Congenit Heart Dis Journal subject: CARDIOLOGIA Year: 2018 Document type: Article Affiliation country: Austria Country of publication: Estados Unidos
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / MELAS Syndrome / Heart Ventricles / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: Congenit Heart Dis Journal subject: CARDIOLOGIA Year: 2018 Document type: Article Affiliation country: Austria Country of publication: Estados Unidos