A3243G mitochondrial mutation associated with polymicrogyria.

Keng, W T

A3243G mitochondrial mutation associated with polymicrogyria. [electronic resource] - Developmental medicine and child neurology Oct 2003 - 704-8 p. digital

Publication Type: Case Reports; Journal Article

0012-1622

10.1017/s0012162203001300 doi


Adolescent
Brain--abnormalities
Calcinosis--pathology
Child
DNA, Mitochondrial--genetics
Diffusion Magnetic Resonance Imaging
Female
Gene Expression--genetics
Humans
MELAS Syndrome--diagnosis
Phenotype
Point Mutation--genetics
Tomography, X-Ray Computed