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K162E - A rare and uncategorized CFTR variant causing cystic fibrosis.
Souza, Edna Lúcia; Ribeiro Mota, Laís; Leite Ferreira de Lima, Renata Lúcia; Horejs Bittencourt, Paloma; Castro Ribeiro Guedes, Virgínia Maria; Salinas, Danieli.
Afiliación
  • Souza EL; Department of Pediatrics, School of Medicine of Bahia, Federal University of Bahia, Salvador, Brazil; Post-Graduation Program in Interactive Processes of Systems and Organs, Institute of Health Sciences, Federal University of Bahia, Salvador, Brazil; Post-Graduation in Medicine and Health, Federal U
  • Ribeiro Mota L; Post-Graduation Program in Interactive Processes of Systems and Organs, Institute of Health Sciences, Federal University of Bahia, Salvador, Brazil.
  • Leite Ferreira de Lima RL; Department of Biology, Institute of Biology, Federal University of Bahia, Salvador, Brazil. Electronic address: fdelima@ufba.br.
  • Horejs Bittencourt P; University Hospital Professor Edgard, Federal University of Bahia, Salvador, Brazil.
  • Castro Ribeiro Guedes VM; University Hospital Professor Edgard, Federal University of Bahia, Salvador, Brazil.
  • Salinas D; Division of Pediatric Pulmonology, Department of Pediatrics, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA. Electronic address: dsalinas@chla.usc.edu.
J Cyst Fibros ; 20(3): 489-491, 2021 05.
Article en En | MEDLINE | ID: mdl-32674983

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Variación Genética / Regulador de Conductancia de Transmembrana de Fibrosis Quística / Fibrosis Quística Idioma: En Revista: J Cyst Fibros Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Variación Genética / Regulador de Conductancia de Transmembrana de Fibrosis Quística / Fibrosis Quística Idioma: En Revista: J Cyst Fibros Año: 2021 Tipo del documento: Article