Ravenscroft et al., 2013
- Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy.
American journal of human genetics
93(1):6-18
Full text @ Am. J. Hum. Genet.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | klhl40a | kelch-like family member 40a |
| Gene | klhl40b | kelch-like family member 40b |