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pro vyhledávání: '"Amin Raazi"'
Autor:
Atieh Mehdizadeh Hakkak, Mohammad Keramatipour, Saeid Talebi, Azam Brook, Jalil Tavakol Afshari, Amin Raazi, Hamid Reza Kianifar
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 16, Iss 8, Pp 917-921 (2013)
Objective(s): More than 1500 registered mutations in cystic fibrosis transmembrane regulator (CFTR) gene are responsible for dysfunction of an ion channel protein and a wide spectrum of clinical manifestations in patients with cystic fibrosis (CF). T
Externí odkaz:
https://doaj.org/article/f2c50e9ea2aa4855970952a7dd7905be
