Found: 1
Select item for more details and to access through your institution.
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.
- Published in:
- Mammalian Genome, 2016, v. 27, n. 3/4, p. 111, doi. 10.1007/s00335-016-9619-x
- By:
- Publication type:
- Article