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Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation.
de Laat, Paul; Koene, Saskia; van den Heuvel, Lambert P W J; Rodenburg, Richard J T; Janssen, Mirian C H; Smeitink, Jan A M.
Affiliation
  • de Laat P; Department of Pediatrics, Nijmegen Centre for Mitochondrial Disorders, Radboud University Nijmegen Medical Centre, Huispost 804, Geert Grooteplein 10, 6500, HB, PO BOX 9101, Nijmegen, The Netherlands. p.laat@cukz.umcn.nl
J Inherit Metab Dis ; 35(6): 1059-69, 2012 Nov.
Article in En | MEDLINE | ID: mdl-22403016
Subject(s)
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Full text: 1 Database: MEDLINE Main subject: DNA, Mitochondrial / Point Mutation / MELAS Syndrome / Deafness / Diabetes Mellitus, Type 2 Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Europa Language: En Journal: J Inherit Metab Dis Year: 2012 Type: Article Affiliation country: Netherlands
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Full text: 1 Database: MEDLINE Main subject: DNA, Mitochondrial / Point Mutation / MELAS Syndrome / Deafness / Diabetes Mellitus, Type 2 Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Europa Language: En Journal: J Inherit Metab Dis Year: 2012 Type: Article Affiliation country: Netherlands