Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy.

Dadgar, Sharareh

Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy. [electronic resource] - Experimental eye research Sep 2006 - 702-6 p. digital

Publication Type: Letter; Research Support, Non-U.S. Gov't

0014-4835

10.1016/j.exer.2006.03.004 doi


Adolescent
Animals
GTP Phosphohydrolases--genetics
Humans
Models, Molecular
Mutation, Missense
Optic Atrophy, Autosomal Dominant--genetics
Protein Structure, Tertiary
Sequence Homology