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Year | Number of Results |
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2020 | 2 |
2021 | 1 |
2024 | 0 |
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A 5-year clinical follow-up study from the Italian National Registry for FSHD.
J Neurol. 2021 Jan;268(1):356-366. doi: 10.1007/s00415-020-10144-7. Epub 2020 Aug 19.
J Neurol. 2021.
PMID: 32813049
Free PMC article.
Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies.
Nikolic A, Jones TI, Govi M, Mele F, Maranda L, Sera F, Ricci G, Ruggiero L, Vercelli L, Portaro S, Villa L, Fiorillo C, Maggi L, Santoro L, Antonini G, Filosto M, Moggio M, Angelini C, Pegoraro E, Berardinelli A, Maioli MA, D'Angelo G, Di Muzio A, Siciliano G, Tomelleri G, D'Esposito M, Della Ragione F, Brancaccio A, Piras R, Rodolico C, Mongini T, Magdinier F, Salsi V, Jones PL, Tupler R.
Nikolic A, et al.
Int J Mol Sci. 2020 Apr 10;21(7):2635. doi: 10.3390/ijms21072635.
Int J Mol Sci. 2020.
PMID: 32290091
Free PMC article.
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