Title of article
Multi-exon out of frame deletion of the FBN1 gene leading to a severe juvenile onset cardiovascular phenotype in Marfan syndrome
Author/Authors
Krishna Kumar Singh، نويسنده , , Diana Elligsen، نويسنده , , Rüdiger Liersch، نويسنده , , Stefanie Schubert، نويسنده , , Brigitte Pabst، نويسنده , , Mine Arslan-Kirchner، نويسنده , , J?rg Schmidtke، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
5
From page
352
To page
356
Abstract
Marfan syndrome is caused by mutations in fibrillin-1, a large gene spanning not, vert, similar 200 kb of genomic DNA on chromosome 15q21. So far, more than 600 different mutations have been identified, accounting for 60–90% of all Marfan syndrome cases, the vast majority being single nucleotide exchanges as well as small deletions and insertions. Only four major rearrangements have been described in the literature so far. We have screened 11 individuals fulfilling the diagnostic criteria of Marfan syndrome but negative for point mutations in the fibrillin-1 gene by SSCP and/or direct sequencing, for large rearrangements. We report here the largest known de novo and out of frame deletion in the fibrillin-1 gene in a patient fulfilling the diagnostic criteria of Marfan syndrome. We identified the deletion breakpoints at the genomic and transcript levels and studied the expression of the mutated allele at the transcript and protein level. We conclude that large rearrangements may account for a non-negligible proportion of all Marfan cases.
Keywords
Large rearrangement , FBN1 , FISH , southern blot , Juvenile onset cardiovascular phenotype , Marfan syndrome
Journal title
Journal of Molecular and Cellular Cardiology
Serial Year
2007
Journal title
Journal of Molecular and Cellular Cardiology
Record number
530057
Link To Document