UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC)

E. M. Hamilton, E. Bertini, L. Kalaydjieva, B. Morar, D. Dojcakova, D. Diodato, N. Wolf, Q. Waisfisz, E. Abbink, M. S. van der Knaap

Research output: Contribution to journalMeeting AbstractAcademic

Original languageEnglish
Pages (from-to)31-32
JournalEuropean Journal of Neurology
Volume25
Publication statusPublished - Jun 2018

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