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AJMG.A.30473
AJMG.A.30473
http://dx.doi.org/10.1002/AJMG.A.30473
Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families.
P356
Q51933512-6576EF65-F21A-41FC-B551-D5AAE27A9C49
P356
AJMG.A.30473
http://dx.doi.org/10.1002/AJMG.A.30473