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Mosab S. Alsaedi
Mosab S. Alsaedi
King Abdulaziz University
Dominance (genetics)
Mutation
Pediatrics
Frameshift mutation
Intensive care medicine
2
Papers
9
Citations
0
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Exome Sequencing and Metabolomic Analysis of A Chronic Kidney Disease and Hearing Loss Patient Family Revealed RMND1 Mutation Induced Sphingolipid Metabolism Defects
2019
Saudi Journal of Biological Sciences
Nagwa E.A. Gaboon
Babajan Banaganapalli
Khalidah Nasser
Mohammed Razeeth
Mosab S. Alsaedi
Omran M. Rashidi
Lereen S. Abdelwehab
Turki S. Alahmadi
Osama Y. Safdar
Jilani P. Shaik
Hani Choudhry
Huda Husain Al-numan
Mohammad Imran Khan
Jumana Y. Al-Aama
Ramu Elango
Noor Ahmad Shaik
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Citations (7)
A Novel Homozygous Frameshift Mutation in CCN6 Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family
2019
Frontiers in Pediatrics
Nagwa E.A. Gaboon
Asia Parveen
Ahmed El Beheiry
Jumana Y. Al-Aama
Mosab S. Alsaedi
Naveed Wasif
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Citations (2)
1