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BCL10 loss-of-function novel mutation leading to atypical severe combined immunodeficiency.
Al-Tamemi, Salem; Alhinai, Zaid; Al-Rahbi, Najwa; Al-Abdawani, Raghad; Al-Yazidi, Laila; Al-Shekaili, Jalila; Al-Kindi, Mahmood; Al-Maawali, Almundher.
Afiliação
  • Al-Tamemi S; Department of Child Health, Sultan Qaboos University Hospital, Muscat, Oman. Electronic address: tamemi@squ.edu.om.
  • Alhinai Z; Department of Child Health, Sultan Qaboos University Hospital, Muscat, Oman.
  • Al-Rahbi N; Department of Child Health, Sultan Qaboos University Hospital, Muscat, Oman.
  • Al-Abdawani R; Department of Child Health, Sultan Qaboos University Hospital, Muscat, Oman.
  • Al-Yazidi L; Department of Child Health, Sultan Qaboos University Hospital, Muscat, Oman.
  • Al-Shekaili J; Department of Microbiology & Immunology, Sultan Qaboos University Hospital, Muscat, Oman.
  • Al-Kindi M; Department of Microbiology & Immunology, Sultan Qaboos University Hospital, Muscat, Oman.
  • Al-Maawali A; Department of Clinical Genetics, Sultan Qaboos University Hospital, Department of Genetics, College of Medicine and Health Sciences, Muscat, Oman.
Clin Immunol ; 241: 109067, 2022 08.
Article em En | MEDLINE | ID: mdl-35750252
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunodeficiência Combinada Severa Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Infant Idioma: En Revista: Clin Immunol Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunodeficiência Combinada Severa Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Infant Idioma: En Revista: Clin Immunol Ano de publicação: 2022 Tipo de documento: Article