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Contribution of common CFTR variants (M470V, T854, and Q1463) to cystic fibrosis in Tunisia: haplotype analysis.
Nefzi, Malek; Fredj, Sondess Hadj; Dabboubi, Rym; Hamouda, Samia; Tebib, Neji; Boussetta, Khedija; Messaoud, Taieb.
Afiliação
  • Nefzi M; Biochemistry laboratory and Molecular laboratory LR00SP03, Children's Hospital, Tunis, Tunisia.
  • Fredj SH; Biochemistry laboratory and Molecular laboratory LR00SP03, Children's Hospital, Tunis, Tunisia.
  • Dabboubi R; Biochemistry laboratory and Molecular laboratory LR00SP03, Children's Hospital, Tunis, Tunisia.
  • Hamouda S; Department of Pediatric C, Children's Hospital, Tunis, Tunisia.
  • Tebib N; Department of Pediatrics, The Rabta Hospital, Tunis, Tunisia.
  • Boussetta K; Department of Pediatric C, Children's Hospital, Tunis, Tunisia.
  • Messaoud T; Biochemistry laboratory and Molecular laboratory LR00SP03, Children's Hospital, Tunis, Tunisia.
Ann Biol Clin (Paris) ; 79(1): 63-68, 2021 Feb 01.
Article em En | MEDLINE | ID: mdl-33589413
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Idioma: En Ano de publicação: 2021 Tipo de documento: Article
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Idioma: En Ano de publicação: 2021 Tipo de documento: Article