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A rare mutation causing autosomal dominant STAT1 deficiency in a South African multiplex kindred with disseminated BCG infection.
Greybe, Leonore; Leung, Daniel; Wieselthaler, Nicole; le Roux, David M; Chan, Koon Wing; Lau, Yu Lung; Eley, Brian.
Afiliación
  • Greybe L; Paediatric Infectious Diseases Unit, Red Cross War Memorial Children's Hospital, Cape Town, South Africa. leonore.greybe@gmail.com.
  • Leung D; Department of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa. leonore.greybe@gmail.com.
  • Wieselthaler N; Department of Paediatrics and Adolescent Medicine, School of Clinical Medicine, Faculty of Medicine, Li Ka Shing, The University of Hong Kong, Hong Kong SAR, China.
  • le Roux DM; Department of Radiology, University of Cape Town, Cape Town, South Africa.
  • Chan KW; Department of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa.
  • Lau YL; Department of Paediatrics and Adolescent Medicine, School of Clinical Medicine, Faculty of Medicine, Li Ka Shing, The University of Hong Kong, Hong Kong SAR, China.
  • Eley B; Department of Paediatrics and Adolescent Medicine, School of Clinical Medicine, Faculty of Medicine, Li Ka Shing, The University of Hong Kong, Hong Kong SAR, China.
BMC Pediatr ; 23(1): 378, 2023 07 29.
Article en En | MEDLINE | ID: mdl-37516851
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacuna BCG / Madres Límite: Child / Female / Humans / Male País/Región como asunto: Africa Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2023 Tipo del documento: Article País de afiliación: Sudáfrica
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacuna BCG / Madres Límite: Child / Female / Humans / Male País/Región como asunto: Africa Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2023 Tipo del documento: Article País de afiliación: Sudáfrica