Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.
Oral Dis
; 22(4): 297-302, 2016 May.
Article
in En
| MEDLINE
| ID: mdl-26762616
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Transcription Factors
/
Base Sequence
/
Sequence Deletion
/
Homeodomain Proteins
/
Amelogenesis Imperfecta
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Adult
/
Child
/
Female
/
Humans
/
Male
Language:
En
Journal:
Oral Dis
Journal subject:
ODONTOLOGIA
Year:
2016
Document type:
Article
Country of publication: