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Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.
Nawaz H, Mujahid, Khan SA, Bibi F, Waqas A, Bari A, Fardous, Khan N, Muhammad N, Khan A, Paracha SA, Alam Q, Kamal MA, Rafeeq MM, Muhammad N, Haq FU, Khan S, Mahmood A, Khan S, Umair M. Nawaz H, et al. Among authors: khan s, khan n, khan a, khan sa. Genes (Basel). 2023 May 19;14(5):1113. doi: 10.3390/genes14051113. Genes (Basel). 2023. PMID: 37239474 Free PMC article.
Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms.
Muhammad N, Hussain SI, Rehman ZU, Khan SA, Jan S, Khan N, Muzammal M, Abbasi SW, Kakar N, Rehman ZU, Khan MA, Mirza MU, Muhammad N, Khan S, Wasif N. Muhammad N, et al. Among authors: khan s, khan n, khan ma, khan sa. Front Neurol. 2023 May 25;14:1168307. doi: 10.3389/fneur.2023.1168307. eCollection 2023. Front Neurol. 2023. PMID: 37305761 Free PMC article.
Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability.
Hussain SI, Muhammad N, Shah SUD, Fardous F, Khan SA, Khan N, Rehman AU, Siddique M, Wasan SA, Niaz R, Ullah H, Khan N, Muhammad N, Mirza MU, Wasif N, Khan S. Hussain SI, et al. Among authors: khan s, khan n, khan sa. BMC Neurol. 2023 Oct 4;23(1):353. doi: 10.1186/s12883-023-03397-y. BMC Neurol. 2023. PMID: 37794328 Free PMC article.
Kissing choroidal sign: A case report.
Doniparthi A, Deutsch AB, Stibbe JD, Khan NM, Palilonis MM. Doniparthi A, et al. Among authors: khan nm. Radiol Case Rep. 2024 May 3;19(8):2934-2936. doi: 10.1016/j.radcr.2024.04.017. eCollection 2024 Aug. Radiol Case Rep. 2024. PMID: 38737180 Free PMC article.
6,313 results