A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy

Utine GE, Haliloglu G, Salanci B, Cetinkaya A, Kiper PO, Alanay Y, Aktas D, Boduroglu K, Alikasifoglu M. A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy. J Child Neurol. 2013 Jul;28(7):926-32.

PubMed ID: 
23611888