
PP88. SPECTRUM OF MUTATIONS IN THE LMNA GENE, CAUSING MUSCULAR DYSTROPHY WITH CONDUCTION SYSTEM DISEASE (EDMD-AD OR LGMD1B) TIHOMIR TODOROV 1, A. Todorova 1, 2, B. Halliger-Keller 2, W. Kress 2, I. Tournev 3, M-C. Dabauvalle 4, I. Kremensky 1, C.R. Mueller 2
1. National Genetic Laboratory, Laboratory of Molecular Pathology, University Hospital of Obstetrics and Gynecology, Sofia Medical University, Sofia, Bulgaria 2. Department of Human Genetics, Biozentrum, University of Wuerzburg, Wuerzburg, Germany 3. Clinic of Neurology, Alexandrovska Hospital, Sofia Medical University, Sofia, Bulgaria 4. Department of Cell and Developmental Biology, Biozentrum, University of Wuerzburg, Wuerzburg, Germany
e-mail: todorova@medfac.acad.bg
*Corresponding Author: page: 87
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MOLECULAR BASIS OF MONOGENIC AND COMPLEX DISEASES
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