2014

Humangenetik, Publikationen 2014

• Müller U: Genetics and neurology. Horizon2020projects, Issue Two, 123 (2014)
• Müller U: Rasante Entwicklung der Gendiagnostik. Editorial. DNP - Der Neurologe & Psychiater, 7–8 (2014)
• Müller U, Winter P, Bolender C, Nolte D: Previously unrecognized missense mutation E126K of PSEN2 segregates with early onset Alzheimer's disease in a family. J Alzheimers Dis. 42(1):109-13 (2014), doi: 10.3233/JAD-140399
• Weber A, Köhler A, Hahn A, Müller U: 8p23.1 duplication syndrome: narrowing of critical interval to 1.80 Mbp. Molec Cytogenet 7:94 (2014)

• Löbbe AM, Kang J-S, Hilker R, Hackstein H, Müller U, Nolte D: A Novel Missense Mutation in AFG3L2 Associated with Late Onset and Slow Progression of Spinocerebellar Ataxia Type 28. J Mol Neurosci 52: 493-496 (2014), doi: 10.1007/s12031-013-0187-1