GABBR2

Publications

Lopes F et al. Identification of novel genetic causes of Rett syndrome-like phenotypes. J Med Genet. 2016;53:190–199 PMID: 26740508.

Samanta D and Zarate YA. Widening phenotypic spectrum of GABBR2 mutation. Acta neurologica Belgica. 2019;119(3), 493-496. PMID: 30707408.

Vuillaume ML et al. A novel mutation in the transmembrane 6 domain of GABBR2 leads to a Rett-like phenotype. Ann Neurol. 2018;83:437–439 PMID: 29369404.

Yoo Y et al. GABBR2 mutations determine phenotype in Rett syndrome and epileptic encephalopathy. Ann Neurol. 2017;82:466–478 4. PMID: 2885670.