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Wiley, Movement Disorders Clinical Practice, 7(7), p. 861-862, 2020

DOI: 10.1002/mdc3.13024

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Cataplexy in patients harboring the KCNMA1 p.N999S mutation

Journal article published in 2020 by Jennifer Heim, Anusha Vemuri, Sara Lewis ORCID, Brandon Guida, Matthew Troester, Sotirios Keros, Andrea Meredith ORCID, Michael C. Kruer
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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