Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.
Orphanet J Rare Dis
; 14(1): 114, 2019 05 23.
Article
in En
| MEDLINE
| ID: mdl-31122244
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Osmotic Fragility
/
Spherocytes
/
Spherocytosis, Hereditary
Type of study:
Diagnostic_studies
Limits:
Aged80
Country/Region as subject:
Asia
Language:
En
Journal:
Orphanet J Rare Dis
Journal subject:
MEDICINA
Year:
2019
Type:
Article