Byla potvrzena nenáhodná asociace alely %22V%22 u varianty M470V s non-F508del mutacemi v genu cystické fibrózy. Tento nález je významný z hlediska DNA diagnostiky (cs)
Background: On the basis of previous findings on random individuals, we hypothesized a preferential association of CF causing mutations with the M allele of the M470V polymorphic site of the CFTR gene. Methods: We have determined the M/V-CF mutation hapl
Background: On the basis of previous findings on random individuals, we hypothesized a preferential association of CF causing mutations with the M allele of the M470V polymorphic site of the CFTR gene. Methods: We have determined the M/V-CF mutation hapl (en)