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Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia

✍ Scribed by Anne Hempelmann; Santosh Kumar; Shanmugakonar Muralitharan; Thomas Sander


Book ID
116768647
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
118 KB
Volume
402
Category
Article
ISSN
0304-3940

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## 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