Mujahid

Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet–Biedl Syndrome

S. Khan, Q. Alam, Shazia Khan, 2023, Genes.

A novel homozygous truncating variant in PPFIBP1 further delineates PPFIBP1‐associated neurodevelopmental disorder

S. Abbas, Ahmed Waqas, M. Aljadani, 2022, International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience.