Denais et al., 2011
- Dymeclin, the gene underlying Dyggve-Melchior-Clausen syndrome, encodes a protein integral to extracellular matrix and golgi organization and is associated with protein secretion pathways critical in bone development.
Human Mutation
32(2):231-239
Full text @ Hum. Mutat.
Marker Type | Symbol | Name |
---|---|---|
Gene | dym | dymeclin |
Gene | hid1b | HID1 domain containing b |