Identification of a novel UROS mutation in a Chinese patient affected by congenital erythropoietic porphyria.
Blood Cells Mol Dis
; 52(1): 57-8, 2014 Jan.
Article
in En
| MEDLINE
| ID: mdl-23953398
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Uroporphyrinogen III Synthetase
/
Exons
/
Porphyria, Erythropoietic
/
Mutation, Missense
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Adult
/
Humans
/
Male
Language:
En
Journal:
Blood Cells Mol Dis
Journal subject:
HEMATOLOGIA
Year:
2014
Document type:
Article