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Paper Details

Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study.
Mov Disord
49
2019
ATM, DYT, DYT-KMT2B dystonia, GNAO1, KMT2B, KMT2B dystonia, KMT2B mutations, KMT2B variant, KMT2B variants, Parkinson and Movement Disorder, childhood-onset dystonia, dystonia, dystonic, generalized dystonia, growth retardation, intellectual disability, neurodevelopmental syndrome, patients, short stature
Author NameAffiliation
Maya TopfInstitute of Structural and Molecular Biology, Birkbeck College, University of London
Nardo NardocciFondazione IRCCS Istituto Neurologico Carlo Besta
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Release 1.2