Severe and rapidly-progressive Lafora disease associated with NHLRC1 mutation: a case report.

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Severe and rapidly-progressive Lafora disease associated with NHLRC1 mutation: a case report.

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Severe and rapidly-progressive ...... HLRC1 mutation: a case report.

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Severe and rapidly-progressive ...... HLRC1 mutation: a case report.

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Severe and rapidly-progressive ...... HLRC1 mutation: a case report.

@en

Severe and rapidly-progressive ...... HLRC1 mutation: a case report.

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Severe and rapidly-progressive ...... HLRC1 mutation: a case report.

@en

Severe and rapidly-progressive ...... HLRC1 mutation: a case report.

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P1476

Severe and rapidly-progressive ...... NHLRC1 mutation: a case report

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P2093

Alfredo D'Aniello

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Pier Paolo Quarato

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Simona Scala

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Veronica Albano

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Yana Ackurina

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P2860

Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism

Lafora disease due to EPM2B mutations: a clinical and genetic study.

Novel NHLRC1 mutations and genotype-phenotype correlations in patients with Lafora's progressive myoclonic epilepsy

Typical progression of myoclonic epilepsy of the Lafora type: a case report.

Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22

Recent advances in the molecular basis of Lafora's progressive myoclonus epilepsy.

Extreme delta brush: a unique EEG pattern in adults with anti-NMDA receptor encephalitis.

Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease.

Lafora disease: severe phenotype associated with homozygous deletion of the NHLRC1 gene.

The progressive myoclonic epilepsies.

P304

1150-1153

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P31

scholarly article

P356

10.1080/00207454.2017.1337012

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P433

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P478

127

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P577

2017-06-12T00:00:00Z

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P698

28556688

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