Post-transcriptional regulation of the creatine transporter gene: Functional relevance of alternative splicing

Author:

Ndika Joseph D.T.,Martinez-Munoz Cristina,Anand Nandaja,van Dooren Silvy J.M.,Kanhai Warsha,Smith Desiree E.C.,Jakobs Cornelis,Salomons Gajja S.

Publisher

Elsevier BV

Subject

Molecular Biology,Biochemistry,Biophysics

Reference45 articles.

1. The genetic landscape of intellectual disability arising from chromosome X;Gécz;Trends Genet.,2009

2. X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome;Salomons;Am. J. Hum. Genet.,2001

3. Arginine:glycine amidinotransferase deficiency: the third inborn error of creatine metabolism in humans;Item;Am. J. Hum. Genet.,2001

4. Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in man;Stöckler;Am. J. Hum. Genet.,1996

5. Inborn metabolic diseases: diagnosis and treatment;Stöckler-ipsiroglu;Mol. Cell. Biochem.,2006

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