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Lereen S. Abdelwehab
Lereen S. Abdelwehab
Ain Shams University
Genetics
Dominance (genetics)
Mutation
Exome sequencing
Sphingolipid
2
Papers
9
Citations
0
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A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients.
2020
Frontiers in Pediatrics
Nagwa E.A. Gaboon
Asia Parveen
Khaled A. Ahmad
Taghreed Shuaib
Jumana Y. Al-Aama
Lereen S. Abdelwehab
Amina Arif
Naveed Wasif
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Citations (2)
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)
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