Cataplexy in patients harboring the KCNMA1 p.N999S mutation

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Movement Disorders Clinical Practice 2020 / 07

Cataplexy in patients harboring the KCNMA1 p.N999S mutation

Heim, Jennifer, Vemuri, Anusha, Lewis, Sara, Guida, Brandon, Troester, Matthew, Keros, Sotirios, Meredith, Andrea, Kruer, Michael C.
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Journal:
Movement Disorders Clinical Practice
DOI:
10.1002/mdc3.13024
Date:
July, 2020
File:
PDF, 919 KB
2020
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