Mental retardation and verbal dyspraxia in a new patient with de novo creatine transporter (SLC6A8) mutation-Reference-Cited by-同舟云学术

Mental retardation and verbal dyspraxia in a new patient with de novo creatine transporter (SLC6A8) mutation

Published:2007 Issue:15 Volume:143A Page:1771-1774
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Battini Roberta,Chilosi Anna,Mei Davide,Casarano Manuela,Alessandrì M. Grazia,Leuzzi Vincenzo,Ferretti Giovanni,Tosetti Michela,Bianchi M. Cristina,Cioni Giovanni

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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5. Arginine:glycine amidinotransferase (AGAT) deficiency in a newborn: Early treatment can prevent phenotypic expression of the disease

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