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Fear of disease progression in carriers of the m.3243A > G mutation.
Custers, José A E; de Laat, Paul; Koene, Saskia; Smeitink, Jan; Janssen, Mirian C H; Verhaak, Christianne.
Afiliação
  • Custers JAE; Department of Medical Psychology, Radboud Center for Mitochondrial Medicine, Radboud University Medical Center, Geert Grooteplein Zuid 10, PO Box 9101, 6500 HB, Nijmegen, The Netherlands. Jose.Custers@radboudumc.nl.
  • de Laat P; Department of Pediatrics, Radboud Center for Mitochondrial Medicine, Radboud University Medical center, Geert Grooteplein Zuid 10, PO Box 9101, 6500 HB, Nijmegen, The Netherlands.
  • Koene S; Department of Pediatrics, Radboud Center for Mitochondrial Medicine, Radboud University Medical center, Geert Grooteplein Zuid 10, PO Box 9101, 6500 HB, Nijmegen, The Netherlands.
  • Smeitink J; Department of Pediatrics, Radboud Center for Mitochondrial Medicine, Radboud University Medical center, Geert Grooteplein Zuid 10, PO Box 9101, 6500 HB, Nijmegen, The Netherlands.
  • Janssen MCH; Department of Internal Medicine, Radboud Center for Mitochondrial Medicine, Radboud University Medical Center, Geert Grooteplein Zuid 10, PO Box 9101, 6500 HB, Nijmegen, the Netherlands.
  • Verhaak C; Department of Medical Psychology, Radboud Center for Mitochondrial Medicine, Radboud University Medical Center, Geert Grooteplein Zuid 10, PO Box 9101, 6500 HB, Nijmegen, The Netherlands.
Orphanet J Rare Dis ; 13(1): 203, 2018 11 13.
Article em En | MEDLINE | ID: mdl-30424784
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Mitocondriais / Mutação Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Mitocondriais / Mutação Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda