Muhammad Ansar
4PUBLICATIONS
19CO-AUTHORS
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Publications (4)
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|Jan 12, 2026
Proceedings of the 12th International Meeting on Neuroacanthocytosis, Cohen Syndrome, and Other VPS13-Related Disorders.Fabrizio Vacca, Binnaz Yalcin, Lars Kaestner
|Oct 25, 2022
KIF1A novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with hereditary sensory and autonomic neuropathy type IIC.Saima Ghafoor, Muhammad Arshad Rafiq, Syed Tahir Abbas Shah
|Aug 10, 2022
A new nonsense mutation in HMX1 in two siblings with oculoauricular syndrome.Muhammad Ansar, Samra Javed, Hafiz Muhammad Azhar Baig
|Mar 11, 2021
Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2.Stylianos E Antonarakis, Aleš Holoubek, Melivoia Rapti
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Frequent Collaborators
1 joint publications
Stylianos E Antonarakis
1 joint publications
Justyna Iwaszkiewicz
1 joint publications
Vincent Zoete
1 joint publications
Callum Wilson
1 joint publications
Christelle Borel
1 joint publications
Olivier Menzel
1 joint publications
Kateřina Kuželová
1 joint publications
Federico A Santoni
1 joint publications
Hafiz Muhammad Azhar Baig
1 joint publications
Mathieu Quinodoz
