A Novel Frameshift Mutation, Deletion of HBB:c.199_202delAAAG [Codon 66/67 (-AAAG)] in ß-Thalassemia Major Patients from the Western Region of Uttar Pradesh, India.
Appl Clin Genet
; 14: 77-85, 2021.
Article
in En
| MEDLINE
| ID: mdl-33688235
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Language:
En
Journal:
Appl Clin Genet
Year:
2021
Type:
Article
Affiliation country:
India