Title : R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian family.

Pub. Date : 2009 Jan

PMID : 19087156






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 BACKGROUND: PLA2G6 mutations are known to be responsible for infantile neuroaxonal dystrophy (INAD) and neurodegeneration with brain iron accumulation (NBIA). Iron phospholipase A2 group VI Homo sapiens