TY  - GEN
AU  - Rouzier,Cécile
AU  - Bannwarth,Sylvie
AU  - Chaussenot,Annabelle
AU  - Chevrollier,Arnaud
AU  - Verschueren,Annie
AU  - Bonello-Palot,Nathalie
AU  - Fragaki,Konstantina
AU  - Cano,Aline
AU  - Pouget,Jean
AU  - Pellissier,Jean-François
AU  - Procaccio,Vincent
AU  - Chabrol,Brigitte
AU  - Paquis-Flucklinger,Véronique
TI  - The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype
SN  - 1460-2156
PY  - 2012///0719
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - DNA Damage
KW  - DNA, Mitochondrial
KW  - genetics
KW  - Female
KW  - GTP Phosphohydrolases
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mitochondrial Myopathies
KW  - complications
KW  - Mitochondrial Proteins
KW  - Mutation, Missense
KW  - Optic Atrophy
KW  - Pedigree
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/brain/awr323
ER  -