Annals of neurology

(Ann Neurol) ISSNs: 0364-5134,

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Title	Authors	Year
Early-onset familial parkinsonism due to POLG mutations.	Davidzon G, Greene P, Mancuso M, Klos KJ, Ahlskog JE, Hirano M, DiMauro S	2006
POLG mutations and Alpers syndrome.	Davidzon G, Mancuso M, Ferraris S, Quinzii C, Hirano M, Peters HL, Kirby D, Thorburn DR, DiMauro S	2005
Sequence analysis of familial PEO shows additional mutations associated with the 752C-->T and 3527C-->T changes in the POLG1 gene.	Lamantea E, Zeviani M	2004
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.	Lamantea E, Tiranti V, Bordoni A, Toscano A, Bono F, Servidei S, Papadimitriou A, Spelbrink H, Silvestri L, Casari G, Comi GP, Zeviani M	2002
POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion.	Naviaux RK, Nguyen KV	2004
Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein.	Sano Y, Date H, Igarashi S, Onodera O, Oyake M, Takahashi T, Hayashi S, Morimatsu M, Takahashi H, Makifuchi T, Fukuhara N, Tsuji S	2004

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