Identification of a novel mutation (525del T) in exon 4 of the CFTR gene in a patient with cystic fibrosis.

Subjects

Subjects :

Base Sequence
Child
Chromosomes, Human, Pair 7
Exons
Female
Humans
Point Mutation
Polymerase Chain Reaction
Sequence Deletion
Cystic Fibrosis genetics
Cystic Fibrosis Transmembrane Conductance Regulator genetics

Details

Language :

English

ISSN :

1098-1004

Volume :

14

Issue :

4

Database :

MEDLINE

Journal :

Human mutation

Publication Type :

Academic Journal

Accession number :

10502789

Full Text :

https://doi.org/10.1002/(SICI)1098-1004(199910)14:4<357::AID-HUMU21>3.0.CO;2-9