Architecture of the Tuberous Sclerosis Protein Complex.
Journal Of Molecular Biology
Ramlaul, Kailash K; Fu, Wencheng W; Li, Hua H; de Martin Garrido, Natàlia N; He, Lin L; Trivedi, Manjari M; Cui, Wei W; Aylett, Christopher H S CHS; Wu, Geng G
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder.
Molecular Autism
Bahl, Samira S; Chiang, Colby C; Beauchamp, Roberta L RL; Neale, Benjamin M BM; Daly, Mark J MJ; Gusella, James F JF; Talkowski, Michael E ME; Ramesh, Vijaya V
Determining the pathogenicity of patient-derived TSC2 mutations by functional characterization and clinical evidence.
European Journal Of Human Genetics : Ejhg
Dunlop, Elaine A EA; Dodd, Kayleigh M KM; Land, Stephen C SC; Davies, Peter A PA; Martins, Nicole N; Stuart, Helen H; McKee, Shane S; Kingswood, Chris C; Saggar, Anand A; Corderio, Isabel I; Medeira, Ana Maria Duarte AM; Kingston, Helen H; Sampson, Julian R JR; Davies, David Mark DM; Tee, Andrew R AR