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Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohort.
Akter H, Rahaman MA, Eshaque TB, Mohamed N, Islam A, Morshed M, Shahin Z, Muhaimin A, Foyzullah AM, Mim RA, Omar FB, Hasan MN, Satsangi D, Ahmed N, Al Saba A, Jahan N, Hossen MA, Mondol MA, Sakib AS, Kabir R, Jahan Chowdhury MS, Shams N, Afroz S, Kanta SI, Bhuiyan SJ, Biswas R, Hanif S, Tambi R, Nassir N, Rahman MM, Duan J, D Børglum A, Amin R, Basiruzzaman M, Kamruzzaman M, Sarker S, Woodbury-Smith M, Uddin KMF, Nabi AHMN, Uddin M. Akter H, et al. Among authors: rahaman ma. Genet Med. 2024 Sep 26;27(1):101282. doi: 10.1016/j.gim.2024.101282. Online ahead of print. Genet Med. 2024. PMID: 39342494 Free article.
Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population.
Sarker S, Eshaque TB, Soorajkumar A, Nassir N, Zehra B, Kanta SI, Rahaman MA, Islam A, Akter S, Ali MK, Mim RA, Uddin KMF, Chowdhury MSJ, Shams N, Baqui MA, Lim ET, Akter H, Woodbury-Smith M, Uddin M. Sarker S, et al. Among authors: rahaman ma. Sci Rep. 2023 Dec 6;13(1):21547. doi: 10.1038/s41598-023-48982-w. Sci Rep. 2023. PMID: 38057384 Free PMC article.
55 results