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Autor:
Santos Júnior, Reinaldo José dos, Silva, Natália Millena, Souza, Pâmella Grasielle Vital Dias de
Publikováno v:
Research, Society and Development; Vol. 10 No. 7; e47610717227
Research, Society and Development; Vol. 10 Núm. 7; e47610717227
Research, Society and Development; v. 10 n. 7; e47610717227
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development; Vol. 10 Núm. 7; e47610717227
Research, Society and Development; v. 10 n. 7; e47610717227
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Cystic fibrosis (CF) is a genetic disease of autosomal recessive profile and is characterized by dysfunction of the CFTR gene, which will affect some organs such as the lungs, pancreas, liver, intestines, and testes, with the lungs being the most cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::47f40ac5ec7f7ba845f1613ab90dbceb
https://rsdjournal.org/index.php/rsd/article/view/17227
https://rsdjournal.org/index.php/rsd/article/view/17227