Reply: The expanding neurological phenotype of DNM1L-related disorders.

Gerber, Sylvie

Reply: The expanding neurological phenotype of DNM1L-related disorders. [electronic resource] - Brain : a journal of neurology 04 2018 - e29 p. digital

Publication Type: Letter; Comment

1460-2156

10.1093/brain/awy027 doi


Dynamins
GTP Phosphohydrolases--genetics
Humans
Microtubule-Associated Proteins--genetics
Mitochondrial Dynamics
Mitochondrial Proteins
Mutation
Optic Atrophy, Autosomal Dominant
Phenotype