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Reply to 'Letter to Editor by Finsterer J and Zarrouk-Mahjoub S: Phenotypic manifestations of the m.8969G>A variant'.
Isohanni, Pirjo; Carroll, Christopher J; Jackson, Christopher B; Pohjanpelto, Max; Lönnqvist, Tuula; Suomalainen, Anu.
Afiliação
  • Isohanni P; Department of Child Neurology, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. pirjo.isohanni@helsinki.fi.
  • Carroll CJ; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland. pirjo.isohanni@helsinki.fi.
  • Jackson CB; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.
  • Pohjanpelto M; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.
  • Lönnqvist T; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.
  • Suomalainen A; Department of Child Neurology, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Neurogenetics ; 19(2): 133-134, 2018 05.
Article em En | MEDLINE | ID: mdl-29480378
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Acidose Láctica / Deficiência Intelectual Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Acidose Láctica / Deficiência Intelectual Idioma: En Ano de publicação: 2018 Tipo de documento: Article