Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy
- 1 September 2009
- journal article
- Published by Elsevier BV in Journal of the American College of Cardiology
- Vol. 54 (10), 930-941
- https://doi.org/10.1016/j.jacc.2009.05.038
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- NCBI GEO: archive for high-throughput functional genomic dataNucleic Acids Research, 2009
- The SR protein family of splicing factors: master regulators of gene expressionBiochemical Journal, 2008
- Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated CardiomyopathyClinical and Translational Science, 2008
- SMN Deficiency Causes Tissue-Specific Perturbations in the Repertoire of snRNAs and Widespread Defects in SplicingCell, 2008
- Splicing in disease: disruption of the splicing code and the decoding machineryNature Reviews Genetics, 2007
- Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing lossNature Genetics, 2005
- Underlying Causes and Long-Term Survival in Patients with Initially Unexplained CardiomyopathyThe New England Journal of Medicine, 2000
- Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System DiseaseThe New England Journal of Medicine, 1999
- Familial dilated cardiomyopathyHeart, 1994
- Echocardiographic measurements in normal subjects from infancy to old age.Circulation, 1980