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Title
A novel custom resequencing array for dilated cardiomyopathy
Authors
Keywords
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Journal
GENETICS IN MEDICINE
Volume 12, Issue 5, Pages 268-278
Publisher
Springer Nature
Online
2010-04-07
DOI
10.1097/gim.0b013e3181d6f7c0
References
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Related references
Note: Only part of the references are listed.- Identification and Functional Characterization of Cardiac Troponin I As a Novel Disease Gene in Autosomal Dominant Dilated Cardiomyopathy
- (2009) Sebastian Carballo et al. CIRCULATION RESEARCH
- Progress With Genetic Cardiomyopathies
- (2009) Ray E. Hershberger et al. Circulation-Heart Failure
- The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy
- (2009) Daniel Vega Møller et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy
- (2009) Katharine M. Brauch et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- ANKRD1, the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene
- (2009) Mousumi Moulik et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy
- (2009) David Hassel et al. NATURE MEDICINE
- Estimating the number of unseen variants in the human genome
- (2009) I. Ionita-Laza et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
- (2008) Sharie B. Parks et al. AMERICAN HEART JOURNAL
- Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy
- (2008) Andreas Perrot et al. BASIC RESEARCH IN CARDIOLOGY
- Array-Based Resequencing Assay for Mutations Causing Hypertrophic Cardiomyopathy
- (2008) S. Waldmuller et al. CLINICAL CHEMISTRY
- Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy
- (2008) Ray E. Hershberger et al. CTS-Clinical and Translational Science
- Mutations causing severe combined immunodeficiency: detection with a custom resequencing microarray
- (2008) Tonya Lebet et al. GENETICS IN MEDICINE
- Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy
- (2008) Christian Geier et al. HUMAN MOLECULAR GENETICS
- A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy
- (2008) Siv Fokstuen et al. HUMAN MUTATION
- Validation of microarray-based resequencing of 93 worldwide mitochondrial genomes
- (2008) Anne Hartmann et al. HUMAN MUTATION
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