A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation.

Bitoun, M

A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation. [electronic resource] - Neurology Jan 2009 - 93-5 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1526-632X

10.1212/01.wnl.0000338624.25852.12 doi


Adult
DNA Mutational Analysis
Dynamin II--genetics
Female
Humans
Muscle, Skeletal--pathology
Mutation--genetics
Myopathies, Structural, Congenital--genetics
Phenotype