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4 resultsUpdated October 20, 2026
1

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NeuroMolecular Medicine 27(1) (2025)

Soma Vankwani; Munazza Raza Mirza; Muhammad Tahir; Muhammad Wasim; Sajid Ali Rajput; Haq Nawaz Khan; Martin R. Larsen; Muhammad Iqbal Choudhary; Fazli Rabbi Awan

2

Whole exome sequencing reveals pathogenic variants in KL and PUDP genes as the cause of intellectual disability in an Iranian family

Gene Reports 24 (2021)

Fatemeh Gholipour; Koh-Ichiro Yoshiura; Mohammadali Hosseinpourfeizi; Naser Elmi; Shahram Teimourian; Reza Safaralizadeh

3

Label free quantitative proteomic profiling of serum samples of intellectually disabled young patients revealed dysregulation of complement coagulation and cholesterol cascade systems

Metabolic Brain Disease 39(5) (2024)

Soma Vankwani; Munazza Raza Mirza; Fazli Rabbi Awan; Muneeza Zafar; Arkadiusz Nawrocki; Muhammad Wasim; Haq Nawaz Khan; Hina Ayesha; Martin Rossel Larsen; Muhammad Iqbal Choudhary

4

Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder

Frontiers in Genetics 14 (2024)

Tayyaba Afsar; Hongxia Fu; Hammal Khan; Zain Ali; Zamrud Zehri; Gohar Zaman; Safdar Abbas; Arif Mahmood; Qamre Alam; Junjian Hu; Suhail Razak; Muhammad Umair