Highly preferential association of NonF508del CF mutations with the M470 allele-Reference-Cited by-同舟云学术

Highly preferential association of NonF508del CF mutations with the M470 allele

Published:2007-01 Issue:1 Volume:6 Page:15-22
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Ciminelli B.M.,Bonizzato A.,Bombieri C.,Pompei F.,Gabaldo M.,Ciccacci C.,Begnini A.,Holubova A.,Zorzi P.,Piskackova T.,Macek M.,Castellani C.,Modiano G.,Pignatti P.F.

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference12 articles.

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3. Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in the European general population;Pompei;Eur J Hum Genet,2006

4. CFTR haplotype backgrounds on normal and mutant CFTR genes;Cuppens;Hum Mol Genet,1994

5. Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations;Dork;Hum Genet,1994

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5. Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling;Andrology;2017-12-07