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Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile.
Clin Epigenetics. 2021 Aug 11;13(1):157. doi: 10.1186/s13148-021-01145-y.
Clin Epigenetics. 2021.
PMID: 34380541
Free PMC article.
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome.
Foroutan A, Haghshenas S, Bhai P, Levy MA, Kerkhof J, McConkey H, Niceta M, Ciolfi A, Pedace L, Miele E, Genevieve D, Heide S, Alders M, Zampino G, Merla G, Fradin M, Bieth E, Bonneau D, Dieterich K, Fergelot P, Schaefer E, Faivre L, Vitobello A, Maitz S, Fischetto R, Gervasini C, Piccione M, van de Laar I, Tartaglia M, Sadikovic B, Lebre AS.
Foroutan A, et al.
Int J Mol Sci. 2022 Feb 5;23(3):1815. doi: 10.3390/ijms23031815.
Int J Mol Sci. 2022.
PMID: 35163737
Free PMC article.
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CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia.
Delle Vedove A, Natarajan J, Zanni G, Eckenweiler M, Muiños-Bühl A, Storbeck M, Guillén Boixet J, Barresi S, Pizzi S, Hölker I, Körber F, Franzmann TM, Bertini ES, Kirschner J, Alberti S, Tartaglia M, Wirth B.
Delle Vedove A, et al.
Cell Mol Life Sci. 2022 Sep 22;79(10):526. doi: 10.1007/s00018-022-04544-3.
Cell Mol Life Sci. 2022.
PMID: 36136249
Free PMC article.
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