Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1).

Poulton, J; Hirano, M; Spinazzola, A; Arenas Hernandez, M; Jardel, C; Lombès, A; Czermin, B; Horvath, R; Taanman, J W; Rotig, A; Zeviani, M; Fratter, C

Poulton, J; Hirano, M; Spinazzola, A; Arenas Hernandez, M; Jardel, C; Lombès, A; Czermin, B; Horvath, R; Taanman, J W; Rotig, A; Zeviani, M; Fratter, C.

Affiliation

Poulton J; University of Oxford, NDOG, The Women's Centre, Oxford OX3 9DU, UK. joanna.poulton@obs-gyn.ox.ac.uk

Biochim Biophys Acta ; 1792(12): 1109-12, 2009 Dec.

Article in En | MEDLINE | ID: mdl-19748572

Subject(s)

DNA, Mitochondrial/genetics; Genes, Mitochondrial/genetics; Mitochondrial Diseases/genetics; Mutation/genetics; Humans; Syndrome

Fulltext

XML

PubMed Links

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Mitochondrial Diseases / Genes, Mitochondrial / Mutation Limits: Humans Language: En Journal: Biochim Biophys Acta Year: 2009 Type: Article Affiliation country: United kingdom

Fulltext

XML

PubMed Links

Search on Google