Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan.
Clin Chim Acta
; 487: 311-317, 2018 Dec.
Article
in En
| MEDLINE
| ID: mdl-30317022
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Spherocytosis, Hereditary
/
Elliptocytosis, Hereditary
/
Erythrocyte Membrane
/
Erythrocytes
Type of study:
Diagnostic_studies
Limits:
Humans
Country/Region as subject:
Asia
Language:
En
Journal:
Clin Chim Acta
Year:
2018
Document type:
Article
Country of publication: