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New mutations in TK2 gene associated with mitochondrial DNA depletion.
Galbiati, Sara; Bordoni, Andreina; Papadimitriou, Dimitra; Toscano, Antonio; Rodolico, Carmelo; Katsarou, Efi; Sciacco, Monica; Garufi, Anastasia; Prelle, Alessandro; Aguennouz, M 'hammed; Bonsignore, Maria; Crimi, Marco; Martinuzzi, Andrea; Bresolin, Nereo; Papadimitriou, Alex; Comi, Giacomo P.
Affiliation
  • Galbiati S; Centro Dino Ferrari, Department of Neurological Sciences, University of Milan, I.R.C.C.S. Ospedale Maggiore Policlinico, Milano, Italy. neurogene@policlinico.mi.it
Pediatr Neurol ; 34(3): 177-85, 2006 Mar.
Article in En | MEDLINE | ID: mdl-16504786
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Collection: 01-internacional Database: MEDLINE Main subject: Thymidine Kinase / DNA, Mitochondrial / DNA Mutational Analysis / Chromosome Aberrations / Mitochondrial Encephalomyopathies / Genes, Recessive Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Pediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2006 Document type: Article Affiliation country: Italia Country of publication: Estados Unidos
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Thymidine Kinase / DNA, Mitochondrial / DNA Mutational Analysis / Chromosome Aberrations / Mitochondrial Encephalomyopathies / Genes, Recessive Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Pediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2006 Document type: Article Affiliation country: Italia Country of publication: Estados Unidos