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Comprehensive Analysis of Genes Associated With Sudden Infant Death Syndrome.
Mehboob R, Kurdi M, Ahmad M, Gilani SA, Khalid S, Nasief H, Mirdad A, Malibary H, Hakamy S, Hassan A, Alaifan M, Bamaga A, Shahzad SA. Mehboob R, et al. Among authors: alaifan m. Front Pediatr. 2021 Oct 15;9:742225. doi: 10.3389/fped.2021.742225. eCollection 2021. Front Pediatr. 2021. PMID: 34722422 Free PMC article.
Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease.
Alharthi AM, Banaganapalli B, Hassan SM, Rashidi O, Al-Shehri BA, Alaifan MA, Alhussaini BH, Alsufyani HA, Alghamdi KS, Nasser KK, Bin-Taleb Y, Elango R, Shaik NA, Saadah OI. Alharthi AM, et al. Among authors: alaifan ma. Front Pediatr. 2022 Jun 15;10:895298. doi: 10.3389/fped.2022.895298. eCollection 2022. Front Pediatr. 2022. PMID: 35783297 Free PMC article.
Rare variant burden analysis from exomes of three consanguineous families reveals LILRB1 and PRSS3 as potential key proteins in inflammatory bowel disease pathogenesis.
Jan RM, Al-Numan HH, Al-Twaty NH, Alrayes N, Alsufyani HA, Alaifan MA, Alhussaini BH, Shaik NA, Awan Z, Qari Y, Saadah OI, Banaganapalli B, Mosli MH, Elango R. Jan RM, et al. Among authors: alaifan ma. Front Med (Lausanne). 2023 May 5;10:1164305. doi: 10.3389/fmed.2023.1164305. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37215724 Free PMC article.
12 results