Title : Functional insights into the creatine transporter.

Pub. Date : 2007

PMID : 18652074






1 Functional Relationships(s)
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Protein Name
Organism
1 CRT is essential for normal brain function as mutations in the CRT gene (SLC6A8) result in X-linked mental retardation, associated with the almost complete lack of creatine in the brain, severe speech and language delay, epilepsy, and autistic behaviour. Creatine solute carrier family 6 (neurotransmitter transporter, creatine), member 8 Mus musculus