Annals of neurology
(Ann Neurol)
ISSNs: 0364-5134,
References in Annals of neurology:
| 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 |