Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes-Reference-Cited by-同舟云学术

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Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes

Published:2000-09-01 Issue:15 Volume:9 Page:2251-2261
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Ganesh S.,Agarwala K. L.,Ueda K.,Akagi T.,Shoda K.,Usui T.,Hashikawa T.,Osada H.,Delgado-Escueta A. V.,Yamakawa K.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/9/15/2251/9818871/092251.pdf

Reference36 articles.

1. Studies in Myoclonus Epilepsy (Lafora Body Form)

2. Extending the capabilities of interphase chromatin mapping

3. Identification of new and common mutations in the EPM2A gene in Lafora disease

4. Isolation and Characterization of Mouse Homologue for the Human Epilepsy Gene,EPM2A

5. Amino Acid Sequences Common to Rapidly Degraded Proteins: The PEST Hypothesis

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1. Gene therapy for Lafora disease in the Epm2a mouse model;Molecular Therapy;2024-07

2. Retinal vascular pathology in a mouse model of Lafora progressive myoclonus epilepsy;Neuroscience Research;2024-07

3. Effect of intracerebroventricular administration of alglucosidase alfa in two mouse models of Lafora disease: Relevance for clinical practice;Epilepsy Research;2024-02

4. Lafora progressive myoclonus epilepsy: Disease mechanism and therapeutic attempts;Journal of Biosciences;2024-01-20

5. Gene replacement therapy for Lafora disease in theEpm2a^-/-mouse model;2023-12-14

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