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Article

Screening of male patients with autism spectrum disorder for creatine transporter deficiency.

Neuropediatrics - 1 Dec 2007

Newmeyer A, deGrauw T, Clark J, Chuck G, Salomons G

Abstract excerpt

Creatine deficiency syndromes (CDS) are newly identified genetic disorders that result in neurological impairment of cognition and communication. The purpose of our study was to screen 100 male subjects with autism spectrum disorder for mutations in the SLC6A8 gene in order to determine the frequency of this genetic disorder in this population. One hundred males ages 3-18 years diagnosed with autism spectrum...

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PMID: 18461508
DOI: 10.1055/s-2008-1065353

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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