Three novel ANO5 missense mutations in Caucasian and Chinese families and sporadic cases with gnathodiaphyseal dysplasia.
Sci Rep
; 7: 40935, 2017 02 08.
Article
in En
| MEDLINE
| ID: mdl-28176803
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Osteogenesis Imperfecta
/
Mutation, Missense
/
Anoctamins
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Aged
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
Language:
En
Journal:
Sci Rep
Year:
2017
Type:
Article
Affiliation country:
China