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pro vyhledávání: '"S. Erfan Hosseini-Asl"'
Autor:
S. Erfan Hosseini-Asl, Jafar Khalafi, Effat Seyedhashemi, Reza Farajollahi, Homa Ahkavan, S. Saied Hosseini-Asl
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-5 (2024)
Abstract Background Cystic fibrosis (CF) is an autosomal recessive inherited life-threatening disease that causes changes in the electrolyte transport system, leading to high absorption of sodium and water. Disease-causing variants of the CFTR gene a
Externí odkaz:
https://doaj.org/article/351d9799c73d4c7b8340b3794ec6e712
