Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families.
Eur J Med Genet
; 62(11): 103561, 2019 Nov.
Article
in En
| MEDLINE
| ID: mdl-30394349
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Dental Enamel Proteins
/
Amelogenesis Imperfecta
/
Genetics, Population
/
Nephrocalcinosis
Type of study:
Screening_studies
Limits:
Adolescent
/
Adult
/
Child
/
Female
/
Humans
/
Male
Country/Region as subject:
America do sul
/
Brasil
Language:
En
Journal:
Eur J Med Genet
Journal subject:
GENETICA MEDICA
Year:
2019
Document type:
Article
Country of publication:
Netherlands