A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia

Overview of attention for article published in American Journal of Human Genetics, May 2015

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RT @JackyGanguly: Nice talk by @neurociencia_br on KMT2B, HPCA and KCTD17 dystonia... KCTD17 vs SGCE in Myoclonus-dystonia🤞 In KCTD17: 1. D…

13 Sep 2020

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Nice talk by @neurociencia_br on KMT2B, HPCA and KCTD17 dystonia... KCTD17 vs SGCE in Myoclonus-dystonia🤞 In KCTD17: 1. Dystonia >>myoclonus 2. Worsen over time 3. No or less responsive to alcohol 4. No imprinting #MDSCongress https://t.co/LIGiecQ4cX

13 Sep 2020

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Open Access UCL Research: A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.http://t.co/lmHZHki1Jh

02 Sep 2015

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PubMed: A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia. http://t.co/lJ5aJrz6lW

21 May 2015

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