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Unveiling genetics of non-syndromic albinism using whole exome sequencing: A comprehensive study of TYR, TYRP1, OCA2 and MC1R genes in 17 families.
Zaman Q, Khan J, Ahmad M, Khan H, Chaudhary HT, Rehman G, Rahman OU, Shah MM, Hussain J, Jamal Q, Khan BT, Khan MA, Sadeeda, Sahar K, Idrees M, Ahmad R, Faisal MS, Khan MI, Khisroon M, Abdulkareem AA, Lee E, Ryu SW, Bibi N, Muthaffar OY, Jelani M, Naseer MI. Zaman Q, et al. Among authors: khan bt, khan ma, khan j, khan mi, khan h. Gene. 2024 Feb 5;894:147986. doi: 10.1016/j.gene.2023.147986. Epub 2023 Nov 11. Gene. 2024. PMID: 37956964
Whole exome sequencing identified five novel variants in CNTN2, CARS2, ARSA, and CLCN4 leading to epilepsy in consanguineous families.
Abdulkareem AA, Zaman Q, Khan H, Khan S, Rehman G, Tariq N, Ahmad M, Owais M, Najumuddin, Muthaffar OY, Bibi F, Khang R, Ryu SW, Naseer MI, Jelani M. Abdulkareem AA, et al. Among authors: khan s, khan h. Front Genet. 2023 Jun 8;14:1185065. doi: 10.3389/fgene.2023.1185065. eCollection 2023. Front Genet. 2023. PMID: 37359369 Free PMC article.
Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type Diseases.
Zaman Q, Khan MA, Sahar K, Rehman G, Khan H, Rehman M, Najumuddin, Ahmad I, Tariq M, Muthaffar OY, Abdulkareem AA, Bibi F, Naseer MI, Faisal MS, Wasif N, Jelani M. Zaman Q, et al. Among authors: khan ma, khan h. Genes (Basel). 2023 Jan 27;14(2):328. doi: 10.3390/genes14020328. Genes (Basel). 2023. PMID: 36833258 Free PMC article.
Utility of scores to predict alcohol use after liver transplant (lt): take them with a grain of salt.
Houston K, Duong N, Sterling RK, Asgharpour A, Bullock S, Weinland S, Keller N, Smirnova E, Khan H, Matherly S, Wedd J, Lee H, Siddiqui M, Patel V, Arias A, Kumaran V, Lee S, Sharma A, Khan A, Imai D, Levy M, Bruno D. Houston K, et al. Among authors: khan h. Liver Transpl. 2024 May 23. doi: 10.1097/LVT.0000000000000407. Online ahead of print. Liver Transpl. 2024. PMID: 38775570
3,645 results