Condition: Hypomyelination, Global Cerebral
rs121434396
in
SLC25A12
gene and
Hypomyelination, Global Cerebral
PMID 24515575
2014 AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate.
PMID 19641205
2009 AGC1 deficiency associated with global cerebral hypomyelination.