Literature DB >> 2210750

The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis.

D J Halley1, H J Veeze, L A Sandkuyl, E Wesby-van Swaay, N H van Damme, W H Deelen, J E Witte, M F Niermeijer.   

Abstract

We tested 190 chromosomes from Dutch cystic fibrosis (CF) patients and carriers for the presence or absence of the major CF mutation delta F508. This mutation was found on 77% of the Dutch CF chromosomes. We observed a significant difference in the distribution of the ages at diagnosis between homozygotes for delta F508 and the other patients. delta F508 homozygotes tend to be identified as patients at neonatal or infantile age. The age at diagnosis of patients with at least one unknown allele, on the other hand, ranged between neonatal and young adult age.

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Year:  1990        PMID: 2210750     DOI: 10.1007/bf02428281

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  1 in total

1.  Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype.

Authors:  H J Veeze; D J Halley; J Bijman; J C de Jongste; H R de Jonge; M Sinaasappel
Journal:  J Clin Invest       Date:  1994-02       Impact factor: 14.808

  1 in total

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