C. Ruivenkamp
AuthID: R-00J-WZT
1
TITLE: Heterozygous variants in SPTBN1 cause intellectual disability and autism Full Text
AUTHORS: Rosenfeld, JA; Xiao, R; Bekheirnia, MR; Kanani, F; Parker, MJ; Koenig, MK; van Haeringen, A; Ruivenkamp, C; Rosmaninho Salgado, J; Almeida, PM; Sa, J; Basto, JP; Palen, E; Oetjens, KF; Burrage, LC; Xia, F; Liu, PF; Eng, CM; Yang, YP; Posey, JE; ...More
PUBLISHED: 2021, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A
AUTHORS: Rosenfeld, JA; Xiao, R; Bekheirnia, MR; Kanani, F; Parker, MJ; Koenig, MK; van Haeringen, A; Ruivenkamp, C; Rosmaninho Salgado, J; Almeida, PM; Sa, J; Basto, JP; Palen, E; Oetjens, KF; Burrage, LC; Xia, F; Liu, PF; Eng, CM; Yang, YP; Posey, JE; ...More
PUBLISHED: 2021, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A
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