Title : Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations.

Pub. Date : 2008 Feb

PMID : 18202189






2 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Mutations in the PLA2G6 gene, which encodes group VIA calcium-independent phospholipase A2 (iPLA(2)beta), were recently identified in patients with infantile neuroaxonal dystrophy (INAD) and neurodegeneration with brain iron accumulation. Iron phospholipase A2 group VI Homo sapiens
2 Mutations in the PLA2G6 gene, which encodes group VIA calcium-independent phospholipase A2 (iPLA(2)beta), were recently identified in patients with infantile neuroaxonal dystrophy (INAD) and neurodegeneration with brain iron accumulation. Iron phospholipase A2 group VI Homo sapiens