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Severer Phenotype in Unverricht-Lundborg Disease (EPM1) Patients Compound Heterozygous for the Dodecamer Repeat Expansion and the c.202C>T Mutation in the CSTB Gene

✍ Scribed by Koskenkorva, Päivi; Hyppönen, Jelena; Äikiä, Marja; Mervaala, Esa; Kiviranta, Tuula; Eriksson, Kai; Lehesjoki, Anna-Elina; Vanninen, Ritva; Kälviäinen, Reetta


Book ID
120300433
Publisher
S. Karger AG
Year
2011
Tongue
English
Weight
210 KB
Volume
8
Category
Article
ISSN
1660-2854

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