Differential 3′ splice site recognition of SMN1 and SMN2 transcripts by U2AF and U2 snRNP
Work
Year: 2009
Type: article
Abstract: Spinal Muscular atrophy is a prevalent genetic disease caused by mutation of the SMN1 gene, which encodes the SMN protein involved in assembly of small nuclear ribonucleoprotein (snRNP) complexes. A p... more
Source: RNA
Authors Mafalda Martins de Araújo, Sophie Bonnal, Michelle L. Hastings, Adrian R. Krainer, Juan Valcárcel
Institutions Centre for Genomic Regulation, Cold Spring Harbor Laboratory, Universitat Pompeu Fabra, Institució Catalana de Recerca i Estudis Avançats
Cites: 62
Cited by: 40
Related to: 10
FWCI: 3.061
Citation percentile (by year/subfield): 81.1
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: bronze