Variability of Creatine Metabolism Genes in Children with Autism Spectrum Disorder

Creatine deficiency syndrome (CDS) comprises three separate enzyme deficiencies with overlapping clinical presentations: arginine:glycine amidinotransferase (GATM gene, glycine amidinotransferase), guanidinoacetate methyltransferase (GAMT gene), and creatine transporter deficiency (SLC6A8 gene, solu...

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Xehetasun bibliografikoak
Argitaratua izan da:Int J Mol Sci
Egile Nagusiak: Cameron, Jessie M., Levandovskiy, Valeriy, Roberts, Wendy, Anagnostou, Evdokia, Scherer, Stephen, Loh, Alvin, Schulze, Andreas
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: MDPI 2017
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Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5578055/
https://ncbi.nlm.nih.gov/pubmed/28758966
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18081665
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