Author

Nousheen

Institution: Quaid-i-Azam University

Observed institution: Quaid-i-Azam University

OpenAlex ID: A5097474308

SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families

2021 · Sabika Firasat, Dur-e-Shawar, et al. · Molecular Biology Reports · 9

Works count: 1

Citation count: 9

H-index: 1

I10-index: