Electro-clinical features and long-term outcomes in guanidinoacetate methyltransferase (GAMT) deficiency

Author:

Yıldız YılmazORCID,Ardıçlı DidemORCID,Göçmen RahşanORCID,Yalnızoğlu DilekORCID,Topçu MeralORCID,Coşkun TurgayORCID,Tokatlı AyşegülORCID,Haliloğlu GöknurORCID

Publisher

Elsevier BV

Reference22 articles.

1. Disorders of creatine transport and metabolism;Longo;Am J. Med. Genet C Semin Med. Genet,2011

2. Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatment;Leuzzi;J. Child Neurol.,2002

3. Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiency;Dhar;Mol. Genet. Metabol.,2009

4. GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis;Mercimek-Mahmutoglu;Neurology,2006

5. Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoring;Stockler-Ipsiroglu;Mol. Genet. Metabol.,2014

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