- Tytuł:
- SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families
- Autorzy:
- Źródło:
- Molecular Biology Reports: An International Journal on Molecular and Cellular Biology. 48(11):7467-7476
Czasopismo naukowe