Histiocytoid Cardiomyopathy
Author:
Publisher
Elsevier
Reference19 articles.
1. Exome sequencing of patients with histiocytoid cardiomyopathy reveals a de novo NDUFB11 mutation that plays a role in the pathogenesis of histiocytoid cardiomyopathy;Shehata;Am J Med Genet A,2015
2. Association of ventricular noncompaction and histiocytoid cardiomyopathy: case report and review of the literature;Planas;Pediatr Dev Pathol,2012
3. Identification of candidate genes for histiocytoid cardiomyopathy (HC) using whole genome expression analysis: analyzing material from the HC registry;Shehata;Pediatr Dev Pathol,2011
4. Histiocytoid cardiomyopathy: does it exist in the fetal-age group?;Jain;Cardiovasc Pathol,2010
5. Histiocytoid cardiomyopathy and ventricular non-compaction in a case of sudden death in a female infant;Edston;Int J Legal Med,2009
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