Shehata et al., 2015
- Exome sequencing of patients with histiocytoid cardiomyopathy reveals a de novo NDUFB11 mutation that plays a role in the pathogenesis of histiocytoid cardiomyopathy.
American journal of medical genetics. Part A
167(9):2114-21
Full text @ Am. J. Med. Genet. A
| Human Disease | Fish | Environment | Evidence Code |
|---|---|---|---|
| infantile histiocytoid cardiomyopathy |