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Disease Info Card
X-linked Creatine Transporter Deficiency
Information about X-linked Creatine Transporter Deficiency: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of X-linked Creatine Transporter Deficiency
Most recent studies have shown that X-linked Creatine Transporter Deficiency shares some biological mechanisms with autistic-disorder, developmental-delay-(disorder), epilepsy, genetic-diseases-x-linked, hereditary-diseases, inborn-errors-of-metabolism, language-delays, language-disorders, mitochondrial-diseases, mitochondrial-myopathies, nervousness, severe-mental-retardation, sex-chromosome-disorders, speech-delay.
Among the many pathways, these few ones have gauged particular interests from scientists studying X-linked Creatine Transporter Deficiency, and have been seen in publications frequently: Creatine Transport, Transport
Quite a number of genes have been found to play important roles in X-linked Creatine Transporter Deficiency, such as CSF2, LAMC2, SLC6A8. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.
Pathways Related to X-linked Creatine Transporter Deficiency
This information is being compiled and will come in a future update
| Creatine Transport | Transport |