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Page 1
Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa.
Latif Z, Chakchouk I, Schrauwen I, Lee K, Santos-Cortez RLP, Abbe I, Acharya A, Jarral A, Ali I, Ullah E, Khan MN, Ali G, Tahir TH, Bamshad MJ, Nickerson DA, Ahmad W, Ansar M, Leal SM; University of Washington Center for Mendelian Genomics (UWCMG) Study Group. Latif Z, et al. Among authors: tahir th. Invest Ophthalmol Vis Sci. 2018 Sep 4;59(11):4552-4557. doi: 10.1167/iovs.18-23849. Invest Ophthalmol Vis Sci. 2018. PMID: 30208423 Free PMC article.
Mutations in the tRNA methyltransferase 1 gene TRMT1 cause congenital microcephaly, isolated inferior vermian hypoplasia and cystic leukomalacia in addition to intellectual disability.
Blaesius K, Abbasi AA, Tahir TH, Tietze A, Picker-Minh S, Ali G, Farooq S, Hu H, Latif Z, Khan MN, Kaindl A. Blaesius K, et al. Among authors: tahir th. Am J Med Genet A. 2018 Nov;176(11):2517-2521. doi: 10.1002/ajmg.a.38631. Epub 2018 Oct 5. Am J Med Genet A. 2018. PMID: 30289604 No abstract available.
In vitro biological screening of the stem of Desmodium elegans.
Khan A, Usman R, Rauf A, Wang ML, Muhammad N, Aman A, Tahir TH. Khan A, et al. Among authors: tahir th. Asian Pac J Trop Biomed. 2013 Sep;3(9):711-5. doi: 10.1016/S2221-1691(13)60143-4. Asian Pac J Trop Biomed. 2013. PMID: 23998011 Free PMC article.