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Publication | Open Access

A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia

DOIFull Paper Access

139

Citations

51

References

2015

Year

Niccolò E. Mencacci, Ignacio Rubio‐Agusti, Anselm A. Zdebik, Friedrich Asmus, Marthe H. R. Ludtmann, Mina Ryten, Vincent Plagnol, Ann‐Kathrin Hauser, Sara Bandrés‐Ciga, Conceição Bettencourt,
The American Journal of Human Genetics

References

YearCitations

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