A novel mouse model of creatine transporter deficiency [v2; ref status: indexed, http://f1000r.es/4zb]

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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Үндсэн зохиолчид:	Laura Baroncelli, Maria Grazia Alessandrì, Jonida Tola, Elena Putignano, Martina Migliore, Elena Amendola, Francesca Zonfrillo, Cornelius Gross, Vincenzo Leuzzi, Giovanni Cioni, Tommaso Pizzorusso
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	F1000 Research Ltd 2015-01-01
Цуврал:	F1000Research
Нөхцлүүд:	Behavioral Neuroscience Neurogenetics
Онлайн хандалт:	http://f1000research.com/articles/3-228/v2
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!