Title : A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability.

Pub. Date : 2016 Aug

PMID : 26416544






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The IMPA1 gene product is responsible for the final step of biotransformation of inositol triphosphate and diacylglycerol, two second messengers. Diglycerides inositol monophosphatase 1 Homo sapiens