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Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients.
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.
Affiliation
  • 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.
  • Mpangase P; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
  • Hauptfleisch M; Sydney Brenner Institute for Molecular Bioscience, 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; Department of Paediatrics, Faculty of Health Sciences, School of Clinical Medicine, Chris Hani Baragwanath Academic Hospital, The University of the Witwatersrand, Johannesburg, South Africa.
  • Immelman M; Genetics Department, Ampath National Reference Laboratory, Centurion, South Africa.
  • Urban M; National Health Laboratory Service Human Genetics Laboratory, Groote Schuur Hospital, Cape Town, South Africa.
  • Krause A; Division of Human Genetics, National Health Laboratory Service and School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa.
Eur J Hum Genet ; 2024 Jul 30.
Article in En | MEDLINE | ID: mdl-39080471
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2024 Document type: Article Affiliation country: South Africa Country of publication: United kingdom
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2024 Document type: Article Affiliation country: South Africa Country of publication: United kingdom