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GeneReviews: Unverricht-Lundborg Disease

GeneReviews: Unverricht-Lundborg Disease

 http://genetests.org/profiles/epm1/index.html Features very detailed genetic information. Forwarding to NCBI Bookshelf : Unverricht-Lundborg Disease Funded by the NIH • Developed at the University of Washington, Seattle [EPM1, Progressive Myoclonus Epilepsy 1, Unverricht-Lundborg Myoclonus Epilepsy] Anna-Elina Lehesjoki, MD, PhD Reetta Kälviäinen, MD, PhD Disease
waiting for hand_moderation GeneTests disease Genetics Testing Laboratories Progressive Myoclonic > Unverricht-Lundborg Disease

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Other links at Progressive Myoclonic > Unverricht-Lundborg Disease
1. GeneReviews: Unverricht-Lundborg Disease

Features very detailed genetic information.
Random site Quote:
Forwarding to NCBI Bookshelf : Unverricht-Lundborg Disease Funded by the NIH • Developed at the University of Washington, Seattle [EPM1, Progressive Myoclonus Epilepsy 1, Unverricht-Lundborg Myoclonus Epilepsy] Anna-Elina Lehesjoki, MD, PhD Reetta Kälviäinen, MD, PhD Disease
waiting for hand_moderation

2. Unverricht-Lundborg Disease : Epilepsy.com

Describes the symptoms and clinical management of the disease.
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Apache/2.2.3 (Red Hat) Server at Port 80 All ad revenues support the mission of the Epilepsy Therapy Project UPDATED: Sun, 10/21/2007 - 9:35pm All ad revenues support the mission of the Epilepsy Therapy Project Unverricht-Lundborg Disease Forward this page to a friend Enter multiple addresses
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3. Unverricht-Lundborg Disease : Epilepsy.com/Professionals

Includes detailed genetic information on Unverricht-Lundborg disease.
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Epilepsy and seizure diagnosis, treatment, and information for Professionals
Search epilepsy.com/professionals: Unverricht-Lundborg Disease Author: Russell Saneto, D.O., Ph.D Unverricht-Lundborg disease (EPM1; OMIM 254800) is the most common of the rare genetically heterogeneous progressive myoclonic epilepsies. Initially described by Unverricht in 1891, , it has also



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