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Cited by in F6Publishing
For: Koko M, Yahia A, Elsayed LE, Hamed AA, Mohammed IN, Elseed MA, Hamad MHA, Babai AM, Siddig RA, Abd Allah ASI, Mohamed M, El-Amin M, Esteves T, Altmüller J, Toliat MR, Thiele H, Nürnberg P, Salih MA, Ahmed AE, Lerche H, Stevanin G. An identical-by-descent novel splice-donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families. Ann Hum Genet 2021;85:186-95. [PMID: 34111303 DOI: 10.1111/ahg.12437] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Stevanin G, Hamed A, Mohamed I, Elseed M, Salih M, Elsadig S, Siddig HE, Nasreldien A, Abdullah MA, Elzubair M, Omer F, Bakhiet A, Abubaker R, Abozar F, Adil R, Emad S, Musallam MA, Eltazi I, Omer Z, Malik H, Mohamed M, Elhassan A, Mohamed E, Ahmed A, Ahmed E, Eltaraifee E, Hussein B, Allah AA, Mohamed L, Nimir M, Elseed OT, Elhassan T, Elbashier A, Alfadul E, Fadul M, Ali K, Taha S, Bushara E, Amin M, koko M, Ibrahim M, Ahmed A, Elsayed L, Yahia A. Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degeneration.. [DOI: 10.21203/rs.3.rs-2219015/v1] [Reference Citation Analysis]
2 Bibbò F, Sorice C, Ferrucci V, Zollo M. Functional Genomics of PRUNE1 in Neurodevelopmental Disorders (NDDs) Tied to Medulloblastoma (MB) and Other Tumors. Front Oncol 2021;11:758146. [PMID: 34745995 DOI: 10.3389/fonc.2021.758146] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]