Arndt et al., 2013
- Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy.
American journal of human genetics
93(1):67-77
Full text @ Am. J. Hum. Genet.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | prdm16 | PR domain containing 16 |
| Gene | skia | v-ski avian sarcoma viral oncogene homolog a |