Novel NKX2–5 Mutations in Diseased Heart Tissues of Patients with Cardiac Malformations
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference35 articles.
1. Molecular evolution of the homeodomain family of transcription factors;Banerjee-Basu;Nucleic Acids Res,2001
2. Intramolecular control of transcriptional activity by the NK2-specific domain in NK-2 homeodomain proteins;Watada;Proc Natl Acad Sci USA,2000
3. Molecular cloning and characterization of human cardiac homeobox gene CSX1;Shiojima;Circ Res,1996
4. Molecular cloning, chromosomal mapping, and characterization of the human cardiac-specific homeobox gene hCsx;Turbay;Mol Med,1996
5. A genetic blueprint for cardiac development;Srivastava;Nature,2000
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