Muhammad Umair

3PUBLICATIONS
3CO-AUTHORS
Haematological tumoursMolecular targetsNeurology and neuromuscular diseases
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Publications (3)

|Oct 03, 2026
A Novel BORCS5 Loss-Of-Function Variant in a Patient With a Rare Neurodevelopmental Disorder.

|Dec 17, 2022
A novel homozygous truncating variant in PPFIBP1 further delineates PPFIBP1-associated neurodevelopmental disorder.

Ahmed Waqas, Romana Liaqat, Sidrah Shaheen

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