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Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. (2017)

First Author: Meyer E

Attributed to: A gene therapy approach to childhood parkinsonism funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.3740

PubMed Identifier: 27992417

Publication URI: http://europepmc.org/abstract/MED/27992417

Type: Journal Article/Review

Volume: 49

Parent Publication: Nature genetics

Issue: 2

ISSN: 1061-4036