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1
s10545-012-9495-9
s10545-012-9495-9
https://scigraph.springernature.com/pub.10.1007/s10545-012-9495-9
Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome.
P2888
Q48490299-C72D1276-423D-4370-9D31-82DC30BDB453
P2888
s10545-012-9495-9
https://scigraph.springernature.com/pub.10.1007/s10545-012-9495-9