No abstract available
MeSH terms
-
Dystonia / drug therapy*
-
Dystonia / genetics*
-
Female
-
GTP Cyclohydrolase / deficiency*
-
GTP Cyclohydrolase / genetics
-
Humans
-
India
-
Infant
-
Magnetic Resonance Imaging
-
Mutation
Substances
-
GCH1 protein, human
-
GTP Cyclohydrolase