High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation-Reference-Cited by-同舟云学术

High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation

Published:2004-07 Issue:1 Volume:75 Page:97-105
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Rosenberg Efraim H.,Almeida Ligia S.,Kleefstra Tjitske,deGrauw Rose S.,Yntema Helger G.,Bahi Nadia,Moraine Claude,Ropers Hans-Hilger,Fryns Jean-Pierre,deGrauw Ton J.,Jakobs Cornelis,Salomons Gajja S.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference26 articles.

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3. X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8;Bizzi;Ann Neurol,2002

4. The C-terminal tail of the GAT-2 GABA transporter contains a novel motif that plays a role in basolateral targeting;Brown;Am J Physiol Cell Physiol,2003

5. Irreversible brain creatine deficiency with elevated serum and urine creatine: a creatine transporter defect?;Cecil;Ann Neurol,2001

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