STAC3disorder: a common cause of congenital hypotonia in Southern African patients

Autor: Essop, Fahmida, Dillon, Bronwyn, Mhlongo, Felicity, Bhengu, Louisa, Naicker, Thirona, Lambie, Lindsay, Smit, Liani, Fieggen, Karen, Lochan, Anneline, Dawson, Jessica, Mpangase, Phelelani, Hauptfleisch, Marc, Scher, Gail, Tabane, Odirile, Immelman, Marelize, Urban, Michael, Krause, Amanda

Publikováno v: European Journal of Human Genetics: EJHG; 20240101, Issue: Preprints p1-10, 10p

Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients.

Autor: Essop F; Division of Human Genetics, National Health Laboratory Service and School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa. fahmida.essop@nhls.ac.za., Dillon B; Division of Human Genetics, National Health Laboratory Service and School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa., Mhlongo F; Division of Human Genetics, National Health Laboratory Service and School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa., Bhengu L; Division of Human Genetics, National Health Laboratory Service and School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa., Naicker T; Division of Genetics, Department of Paediatrics, Inkosi Albert Luthuli Central Hospital and University of KwaZulu-Natal, Durban, South Africa., Lambie L; Genetics Department, Ampath National Reference Laboratory, Centurion, South Africa., Smit L; Department of Obstetrics and Gynaecology, Faculty of Medicine and Health Sciences, Stellenbosch University, Stellenbosch, South Africa., Fieggen K; Division of Human Genetics and Department of Medicine, University of Cape Town, Cape Town, South Africa., Lochan A; Division of Human Genetics, National Health Laboratory Service and School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa., Dawson J; Division of Human Genetics, National Health Laboratory Service and School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa.; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada., Mpangase P; Sydney Brenner Institute for Molecular Bioscience, University of the Witwatersrand, Johannesburg, South Africa., Hauptfleisch M; Department of Paediatrics, Faculty of Health Sciences, School of Clinical Medicine, Chris Hani Baragwanath Academic Hospital, The University of the Witwatersrand, Johannesburg, South Africa., Scher G; Department of Paediatrics, Faculty of Health Sciences, School of Clinical Medicine, Chris Hani Baragwanath Academic Hospital, The University of the Witwatersrand, Johannesburg, South Africa., Tabane O; Genetics Department, Ampath National Reference Laboratory, Centurion, South Africa., Immelman M; National Health Laboratory Service Human Genetics Laboratory, Groote Schuur Hospital, Cape Town, South Africa., Urban M; Division of Human Genetics, National Health Laboratory Service and School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa.; Department of Obstetrics and Gynaecology, Faculty of Medicine and Health Sciences, Stellenbosch University, Stellenbosch, South Africa., Krause A; Division of Human Genetics, National Health Laboratory Service and School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa.

Publikováno v: European journal of human genetics : EJHG [Eur J Hum Genet] 2024 Jul 30. Date of Electronic Publication: 2024 Jul 30.