Clinical characteristics of paroxysmal n
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Elka Stefanova; Ana Djarmati; Dragana Momčilović; Nataša Dragašević; Marina Svet
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Article
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2006
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John Wiley and Sons
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English
⚖ 105 KB
## Abstract The aim of this study was to describe the clinical features of a large Serbian family with paroxysmal nonkinesigenic dyskinesia (PNKD) and one of the two previously described mutations in the __Myofibrillogenesis regulator 1__ gene (__MR‐1__), which causes an alanine‐to‐valine substitut