Gene diagnosis of alkaptonuria in an infant.
- Author:
Man HU
1
;
Hong-Wei MA
;
Yang LUO
;
Lin WANG
;
Ying SONG
;
Fang LI
Author Information
- Publication Type:Case Reports
- MeSH: Alkaptonuria; diagnosis; genetics; therapy; Homogentisate 1,2-Dioxygenase; genetics; Humans; Infant; Male
- From: Chinese Journal of Contemporary Pediatrics 2012;14(10):796-797
- CountryChina
- Language:Chinese
