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J.AJHG.2015.04.008
J.AJHG.2015.04.008
http://dx.doi.org/10.1016/J.AJHG.2015.04.008
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia
P356
Q24337555-E8B7CE36-2A33-493F-92B2-271A9E682245
P356
J.AJHG.2015.04.008
http://dx.doi.org/10.1016/J.AJHG.2015.04.008