Treatment experience in two adults with creatinfe transporter deficiency
Author:
Funder
Stichting Metakids
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference35 articles.
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3. X-linked creatine transporter (SLC6A8) mutations in about 1% of males with mental retardation of unknown etiology;Clark;Hum. Genet.,2006
4. High prevalence of SLC6A8 deficiency in X-linked mental retardation;Rosenberg;Am. J. Hum. Genet.,2004
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