Muhammad Muzammal
3PUBLICATIONS
1CO-AUTHORS
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Publications (3)
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|Feb 13, 2026
A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.Sana Fatima, Dong Sun, Jianguo Han
|Oct 01, 2025
Expanding the ethnic and clinical spectrum of the IDS c.1122C>T mutation: first report from Pakistan.Sana Fatima, Hunza Malik, Aftab Ali
|Nov 26, 2021
Mutation screening of multiple Pakistani MCPH families revealed novel and recurrent protein-truncating mutations of ASPM.Sadam Hussain, Amjad Nawaz, Malaika Hamid
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