Muhammad Imran Naseer
5PUBLICATIONS
13CO-AUTHORS
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Publications (5)
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|Jan 19, 2024
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis.Osama Y Muthaffar, Asma Alqarni, Jumana A Shafei
|Dec 09, 2022
KIF4 regulates neuronal morphology and seizure susceptibility via the PARP1 signaling pathway.Yuansong Wan, Momo Morikawa, Manatsu Morikawa
|Sep 29, 2020
Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family.Muhammad Ismail Khan, Muhammad Latif, Maria Saif
|Nov 05, 2018
A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family.Angham Abdulrahman Abdulkareem, Khalid Omar Abulnaja, Mohammad M Jan
|Oct 14, 2018
A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy.Muhammad Imran Naseer, Mohammad Khalid Alwasiyah, Angham Abdulrahman Abdulkareem
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Frequent Collaborators
1 joint publications
Muhammad Latif
1 joint publications
Hafiz Muhammad Jafar Hussain
1 joint publications
Musharraf Jelani
1 joint publications
Yuansong Wan
1 joint publications
Momo Morikawa
1 joint publications
Manatsu Morikawa
1 joint publications
Suguru Iwata
1 joint publications
Yosuke Tanaka
1 joint publications
Nobutaka Hirokawa
1 joint publications
Osama Y Muthaffar
