Title : X-linked creatine transporter deficiency results in prolonged QTc and increased sudden death risk in humans and disease model.

Pub. Date : 2021 Oct

PMID : 34050321






2 Functional Relationships(s)
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1 PURPOSE: Creatine transporter deficiency (CTD) is a rare X-linked disorder of creatine transport caused by pathogenic variants in SLC6A8 (Xq28). Creatine solute carrier family 6 (neurotransmitter transporter, creatine), member 8 Mus musculus
2 PURPOSE: Creatine transporter deficiency (CTD) is a rare X-linked disorder of creatine transport caused by pathogenic variants in SLC6A8 (Xq28). Creatine solute carrier family 6 (neurotransmitter transporter, creatine), member 8 Mus musculus