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Autor:
E. L. S. de Souza, M. A. Santana, Fabio R. Faucz, L. Culpi, John A. Phillips, Francisco J.C. Reis, Salmo Raskin, Lilian Pereira-Ferrari, R. B. de Alexandre, Diego S. Souza, Vanessa Santos Sotomaior
Publikováno v:
Genetica. 145(1)
Cystic fibrosis (CF) is a common autosomal recessive disorder, being the p.F508del the most frequent mutation. Also, a nearby restriction fragment length polymorphism (RFLP) named XK (KM19 and XV2C) is non-randomly associated with specific CF alleles