Detection of more than 91% cystic fibrosis mutations in a sample of the population from Reunion Island and identification of two novel mutations (A309G, S1255L) and one novel polymorphism (L49L)

Saved in:
Bibliographic Details
Published inClinical genetics Vol. 54; no. 5; pp. 437 - 439
Main Authors Cwtuult, F., Stefjrrrnn, J., Viduud, D., Botrsquet, S., Lestire, F., Renotiil, M., MeDonell, N., Feingold, J., Belrljord, C., Bienvenu, T.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.11.1998
Subjects
Alanine - genetics
Cystic Fibrosis - genetics
Cystic Fibrosis Transmembrane Conductance Regulator - genetics
France
Glycine - genetics
Humans
Leucine - genetics
Mutation, Missense
Polymorphism, Genetic
Serine - genetics
France
Online AccessGet full text

Cover

More Information
Bibliography:ark:/67375/WNG-3VX203S5-7
istex:CD6671F1AED20A19F7B8449D4AD7D80C6A9FE19F
ArticleID:CGE437
SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ISSN:0009-9163
1399-0004
DOI:10.1111/j.1399-0004.1998.tb03760.x