Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing.

ABSTRACT:

Background

Currently molecular diagnostic laboratories focus only on the identification of large deletion and duplication mutations (spanning one exon or more) for Duchenne Muscular Dystrophy (DMD) yielding 65% of causative mutations. These mutations are detected by an existing set of multiplexed polymerase chain reaction (PCR) primer pairs. Due to the large size of the dystrophin gene (79 exons), finding point mutations (substitutions, deletions or insertions of one or several nucleotides) has been prohibitively expensive and laborious. The aim of this project was to develop an effective and convenient method of finding all, or most, mutations in the dystrophin gene with only a moderate increase in cost.

Results

Using denaturing high performance liquid chromatography (DHPLC

SUBMITTER: Bennett RR 

PROVIDER: S-EPMC59832 | biostudies-literature | 2001

REPOSITORIES: biostudies-literature