A novel mouse model of creatine transporter deficiency [v1; ref status: indexed, http://f1000r.es/4f8]

A novel mouse model of creatine transporter deficiency [v1; ref status: indexed, http://f1000r.es/4f8]

Mutations in the creatine (Cr) transporter (CrT) gene lead to cerebral creatine deficiency syndrome-1 (CCDS1), an X-linked metabolic disorder characterized by cerebral Cr deficiency causing intellectual disability, seizures, movement  and behavioral disturbances, language and speech impairment ( OMI...

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Bibliographic Details
Main Authors: Laura Baroncelli, Maria Grazia Alessandrì, Jonida Tola, Elena Putignano, Martina Migliore, Elena Amendola, Cornelius Gross, Vincenzo Leuzzi, Giovanni Cioni, Tommaso Pizzorusso
Format: Article
Language:English
Published: F1000 Research Ltd 2014-09-01
Series:F1000Research
Subjects:
Behavioral Neuroscience
Neurogenetics
Online Access:http://f1000research.com/articles/3-228/v1

Internet

http://f1000research.com/articles/3-228/v1

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