Advance in molecular diagnosis of familial hypercholesterolemia in the Czech population: identification and characterization of large rearrangements in LDLR gene

Warning

This publication doesn't include Faculty of Economics and Administration. It includes Faculty of Medicine. Official publication website can be found on muni.cz.
Authors

GOLDMANN R. ZAPLETALOVA P. LETOCHA O. VYROUBALOVA L. PORUBKOVA J. TICHY L. FREIBERGER T. KOZÁK L.

Year of publication 2007
Type Article in Proceedings
Conference Sborník abstrakt 22. pracovní dny Dědičné metabolické poruchy
MU Faculty or unit

Faculty of Medicine

Citation
Field Genetics and molecular biology
Keywords Familial hyprecholesterolémia; LDLR gene; MLPA
Description Familial hypercholesterolemia (FH) is an autosomal dominant disorder caused by mutations in the gene encoding the low density lipoprotein receptor (LDLR). Mutations in the LDLR gene were diagnosed using exon by exon screening methods based on individual exon amplification, DHPLC analysis and sequencing. Recently, a novel method for genomic quantification, Multiplex Ligation-dependent Probe Amplification (MLPA), has been developed. In order to explore the possibility that whole exon deletions or duplications could be the causative mutation on some yet uncharacterized mutant LDLR alleles, we used MLPA technique in this study.Six different large deletions and three duplications were found, 3 of which (EX9_15del-14kb, EX9_14del-9.5kb and EX2_6dup-8.5kb) were prevalent in FH individuals from the Czech population.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.