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Damásio J, Santos M, Samões R, et al. Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype. Clin Genet. 2021;100(6):743-747doi: 10.1111/cge.14055.
Damásio, J., Santos, M., Samões, R., Araújo, M., Macedo, M., Sardoeira, A., Cavaco, S., Freitas, J., Barros, J., Oliveira, J., & Sequeiros, J. (2021). Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype. Clinical genetics, 100(6), 743-747. https://doi.org/10.1111/cge.14055
Damásio, Joana, et al. "Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype." Clinical genetics vol. 100,6 (2021): 743-747. doi: https://doi.org/10.1111/cge.14055
Damásio J, Santos M, Samões R, Araújo M, Macedo M, Sardoeira A, Cavaco S, Freitas J, Barros J, Oliveira J, Sequeiros J. Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype. Clin Genet. 2021 Dec;100(6):743-747. doi: 10.1111/cge.14055. Epub 2021 Sep 08. PMID: 34477219.
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