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Article

X-Linked Creatine-Transporter Gene (SLC6A8) Defect: A New Creatine-Deficiency Syndrome

1 Jun 2001

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 11326334
DOI: 10.1086/320595

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X-Linked Creatine-Transporter Gene (SLC6A8) Defect: A New Creatine-Deficiency SyndromePMID 11326334Read ↗

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Estimated carrier frequency of creatine transporter deficiency in females in the general population using functional characterization of novel missense variants in the SLC6A8 gene.Semantic proximity Read ↗

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