MAGEL2 gene
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (2)
Papers in which this entity is mentioned.
- Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. (2013)
- Central precocious puberty caused by mutations in the imprinted gene MKRN3. (2013)
Merged raw entities (1)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| magel2 | gene | 2 | 4 |