A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families.

Bouhouche, Ahmed

A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families. [electronic resource] - The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques Nov 2007 - 421-6 p. digital

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

0317-1671

10.1017/s0317167100007290 doi


Adolescent
Age of Onset
Amino Acid Sequence
Charcot-Marie-Tooth Disease--genetics
Child
Female
Humans
Male
Morocco--epidemiology
Mutation
Nerve Tissue Proteins--genetics
Pedigree