Alkaptonuria in Turkey: Clinical and molecular characteristics of 66 patients.
Eur J Med Genet
; 64(5): 104197, 2021 May.
Article
in En
| MEDLINE
| ID: mdl-33746036
Full text:
1
Database:
MEDLINE
Main subject:
Phenotype
/
Alkaptonuria
/
Homogentisate 1,2-Dioxygenase
Type of study:
Clinical_trials
/
Diagnostic_studies
/
Prognostic_studies
/
Screening_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
/
Middle aged
Country/Region as subject:
Asia
Language:
En
Journal:
Eur J Med Genet
Journal subject:
GENETICA MEDICA
Year:
2021
Type:
Article
Affiliation country:
Turkey