Refining the phenotype of Unverricht-Lundborg disease (EPM1): a population-wide Finnish study.
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Therapeutic Developments for Tics and Myoclonus.Has Progress Been Made in Progressive Myoclonic Epilepsy (EPM1)?Update on pharmacological treatment of Progressive Myoclonus Epilepsies.Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties.First Molecular Diagnosis of a Patient with Unverricht-Lundborg Disease in Korea
P2860
Refining the phenotype of Unverricht-Lundborg disease (EPM1): a population-wide Finnish study.
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2015 nî lūn-bûn
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Refining the phenotype of Unve ...... population-wide Finnish study.
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Refining the phenotype of Unverricht-Lundborg disease
@nl
type
label
Refining the phenotype of Unve ...... population-wide Finnish study.
@en
Refining the phenotype of Unverricht-Lundborg disease
@nl
prefLabel
Refining the phenotype of Unve ...... population-wide Finnish study.
@en
Refining the phenotype of Unverricht-Lundborg disease
@nl
P2093
P1433
P1476
Refining the phenotype of Unve ...... population-wide Finnish study.
@en
P2093
Esa Mervaala
Jelena Hyppönen
Marja Äikiä
Nils Danner
Petro Julkunen
Päivi Koskenkorva
Reetta Kälviäinen
Ritva Vanninen
Tarja Joensuu
P304
P356
10.1212/WNL.0000000000001466
P407
P577
2015-03-13T00:00:00Z