Wyniki wyszukiwania

Sortuj według:

Ogranicz wyniki do:

Carrier status for 3 most frequent CFTR mutations in Polish PCD-KS patients: lack of association with the primary ciliary dyskinesia phenotype

100%

Skrzypczak U., Rutkiewicz E., Pogorzelski A., Witt M., Zietkiewicz E.

Journal of Applied Genetics

2007

tom 48

nr 1

85-88

We screened a large group of primary ciliary dyskinesia/Kartagener syndrome (PCD/KS) patients and their siblings (148 patients from 126 unrelated families) for the presence of the CFTR mutations that are most frequently found in the Polish population: the severe F508del and 2,3del21kb, and the mild 3849+l0kbC > T. No statistically significant increase in the frequency of these mutations was found in the studied group, as compared with the general population. This is consistent with an earlier observation in another population and indicates that the status of being a carrier of any of these CFTR mutations should not be considered as an important risk factor in PCD/KS pathogenesis.

Neutral haplotype diversity in the CFTR gene in healthy Polish population and in cystic fibrosis patients carrying four most frequent CF mutations

86%

Voelkel K., Joskowiak A., Nawracala M., Rutkiewicz E., Skrzypczak U., Witt M., Zietkiewicz E.

Acta Biochimica Polonica

2006

tom 53

nr Supplement 1

Ograniczanie wyników

1 Acta Biochimica Polonica

1 Journal of Applied Genetics

2 Rutkiewicz E.

2 Skrzypczak U.

2 Witt M.

2 Zietkiewicz E.

1 Joskowiak A.

1 Nawracala M.

1 Pogorzelski A.

1 Voelkel K.

1 2007

1 2006

Wyniki wyszukiwania

Carrier status for 3 most frequent CFTR mutations in Polish PCD-KS patients: lack of association with the primary ciliary dyskinesia phenotype

Neutral haplotype diversity in the CFTR gene in healthy Polish population and in cystic fibrosis patients carrying four most frequent CF mutations