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Clinical Epigenetics|April 10, 2026
Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signaturesAsuman Koparir, Jennifer Kerkhof, Jessica Rzasa, et al.Annals of Neurology|March 31, 2015
Oligoclonal bands predict multiple sclerosis in children with optic neuritisNicole Heussinger, Evangelos Kontopantelis, Janina Gburek-Augustat, et al.American Journal of Human Genetics|October 24, 2003
Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathyJan Senderek, Carsten Bergmann, Claudia Stendel, et al.Nature Genetics|August 6, 2013
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and miceAnnika Keller, Ana Westenberger, Maria J Sobrido, et al.Pageof 3