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For: Freitas JL, Vale TC, Barsottini OGP, Pedroso JL. Expanding the Phenotype of Dystonia-Deafness Syndrome Caused by ACTB Gene Mutation. Mov Disord Clin Pract 2020;7:86-7. [PMID: 31970217 DOI: 10.1002/mdc3.12854] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 Lange LM, Gonzalez-Latapi P, Rajalingam R, Tijssen MAJ, Ebrahimi-Fakhari D, Gabbert C, Ganos C, Ghosh R, Kumar KR, Lang AE, Rossi M, van der Veen S, van de Warrenburg B, Warner T, Lohmann K, Klein C, Marras C; on behalf of the Task Force on Genetic Nomenclature in Movement Disorders. Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update. Mov Disord 2022. [PMID: 35481685 DOI: 10.1002/mds.28982] [Reference Citation Analysis]
2 Zavala L, Ziegler G, Morón DG, Garretto N. Dystonia-Deafness Syndrome: ACTB Pathogenic Variant in an Argentinean Family. Mov Disord Clin Pract 2022;9:122-4. [PMID: 35005077 DOI: 10.1002/mdc3.13358] [Reference Citation Analysis]
3 Ahmadi M, Pashangzadeh S, Moraghebi M, Sabetian S, Shekari M, Eini F, Salehi E, Mousavi P. Construction of circRNA-miRNA-mRNA network in the pathogenesis of recurrent implantation failure using integrated bioinformatics study. J Cell Mol Med 2021. [PMID: 33960101 DOI: 10.1111/jcmm.16586] [Reference Citation Analysis]
4 Vanslembrouck B, Ampe C, Hengel J. Time for rethinking the different β‐actin transgenic mouse models? Cytoskeleton 2020;77:527-43. [DOI: 10.1002/cm.21647] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 Chouksey A, Pandey S. ATP1A3 mutation presenting as CAPOS syndrome + dystonia phenotype. Parkinsonism Relat Disord 2020;78:192-4. [PMID: 32576493 DOI: 10.1016/j.parkreldis.2020.05.029] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
6 Hampshire K, Martin PM, Carlston C, Slavotinek A. Baraitser-Winter cerebrofrontofacial syndrome: Report of two adult siblings. Am J Med Genet A 2020;182:1923-32. [PMID: 32506774 DOI: 10.1002/ajmg.a.61637] [Reference Citation Analysis]