Liaqat Ali

Homozygosity Mapping and Targeted Sanger Sequencing Reveal Genetic Defects Underlying Inherited Retinal Disease in Families from Pakistan

A. D. den Hollander, F. Cremers, N. Waheed, 2015, PloS one.

Role of 19 SNPs in 10 Genes with Type 2 Diabetes in the Pakistani Population.

D. Roshandel, S. Bano, Maleeha Maria, 2022, Gene.

Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency.

S. Antonarakis, C. Pournaras, C. Rivolta, 2019, Human molecular genetics.