Sheraz Khan
4PUBLICATIONS
33CO-AUTHORS
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Publications (4)
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|Jul 30, 2023
Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders.Reza Maroofian, Rauan Kaiyrzhanov, Elisa Cali
|Oct 23, 2021
A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family.Syeda Seema Waseem, Abubakar Moawia, Birgit Budde
|Aug 27, 2021
A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family.Shafaq Ramzan, Stephanie Tennstedt, Muhammad Tariq
|Jun 02, 2021
Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ.Ehtisham Ul Haq Makhdoom, Syeda Seema Waseem, Maria Iqbal
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Frequent Collaborators
3 joint publications
Muhammad Tariq
3 joint publications
Peter Nürnberg
2 joint publications
Birgit Budde
2 joint publications
Ayaz Khan
2 joint publications
Muhammad Sajid Hussain
1 joint publications
Uzma Abdullah
1 joint publications
Saadia Maryam Saadi
1 joint publications
Emrah Kaygusuz
1 joint publications
Iram Anjum
1 joint publications
Hafiza Noor Ul Ayan
