Holt et al., 2019
- De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies.
American journal of human genetics
105(3):640-657
Full text @ Am. J. Hum. Genet.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | fbxw11a | F-box and WD repeat domain containing 11a |
| Gene | fbxw11b | F-box and WD repeat domain containing 11b |
| Gene | tcf7l1a | transcription factor 7 like 1a |