Work

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

Year: 2021

Type: article

Study design: Observational Study

Source: Molecular Biology Reports

DOI: 10.1007/s11033-021-06765-4

Authors: Sabika Firasat, Dur-e-Shawar, Wajid Ali Khan, Ume Sughra, Nousheen, Haiba Kaul, Shagufta Naz, Bushra Noreen, Rutaba Gul, Kiran Afshan

Institutions: Quaid-i-Azam University, Al-Shifa Trust Eye Hospital, University of Veterinary and Animal Sciences, Lahore College for Women University

Language: English

Topic: Corneal surgery and disorders

Subfield: Ophthalmology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Quaid-i-Azam University, Higher Education Commission, Pakistan

Awards: G6940855412, G8639653433, G902201133

OpenAlex ID: W3205962223

FWCI: 1.485

Cites: 41

Cited by: 9

Related to: 10