X-linked creatine transporter (SLC6A8) mutations in about 1% of males with mental retardation of unknown etiology

Overview of attention for article published in Human Genetics, April 2006

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German

Kreatin-Transporter-Defekt

Cited by user Falko Krügel on 17 Nov 2022

Der Kreatin-Transporter-Defekt (kurz CTD) ist eine sehr seltene, zu den Syndromalen X-chromosomalen mentalen Retardierungen zählende angeborene Störung des Kreatin-Transpo…

English

SLC6A8

Cited by user ProteinBoxBot on 20 Dec 2007

Sodium- and chloride-dependent creatine transporter 1 is a protein that in humans is encoded by the SLC6A8 gene.

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