Functional Characterization of Putative Novel Splicing Mutations in the Cardiomyopathy-Causing Genes-Reference-Cited by-同舟云学术

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Functional Characterization of Putative Novel Splicing Mutations in the Cardiomyopathy-Causing Genes

Published:2015-07 Issue:7 Volume:34 Page:489-496
ISSN:1044-5498
Container-title:DNA and Cell Biology
language:en
Short-container-title:DNA and Cell Biology

Author:

Millat Gilles¹²,Lafont Estèle²,Nony Séverine¹,Rouvet Isabelle³,Bozon Dominique¹

Affiliation:

1. Laboratoire de Cardiogénétique Moléculaire, Centre de Biologie et Pathologie Est–Hospices Civils de Lyon, Bron, France.

2. EA4612, Université Claude Bernard Lyon 1, Lyon, France.

3. Centre de Biotechnologie Cellulaire, CBPE–Hospices Civils de Lyon, Bron, France.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Genetics,Molecular Biology,General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/dna.2015.2842

Reference26 articles.

1. Functional Classification of BRCA2 DNA Variants by Splicing Assays in a Large Minigene with 9 Exons

2. Regulation of gene expression programmes by serine–arginine rich splicing factors

3. Splicing in action: assessing disease causing sequence changes

4. Exon Recognition in Vertebrate Splicing

5. U1 snRNA mis-binding: a new cause of CMT1B

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