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XB-ART-53955
Ann Neurol. September 1, 2017; 82 (3): 466-478.

GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.

Yoo Y , Jung J , Lee YN , Lee Y , Cho H , Na E , Hong J , Kim E , Lee JS , Lee JS , Hong C , Park SY , Wie J , Miller K , Shur N , Clow C , Ebel RS , DeBrosse SD , Henderson LB , Willaert R , Castaldi C , Tikhonova I , Bilg├╝var K , Mane S , Kim KJ , Hwang YS , Lee SG , So I , Lim BC , Choi HJ , Seong JY , Shin YB , Jung H , Chae JH , Choi M .


Abstract


PubMed ID: 28856709
Article link: Ann Neurol.

Genes referenced: gabbr2 mecp2



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