In silico and in vivo models for Qatari-specific classical homocystinuria as basis for development of novel therapiesHesham M. Ismail, Gheyath K. Nasrallah, Nura A. Mohamed et al.|Human Mutation|2018Cited by 21
Burden of Mendelian disorders in a large Middle Eastern biobankWaleed Aamer, Shafeeq Poolat, Aljazi Al-Maraghi et al.|Genome Medicine|2024Cited by 21