PME of Unverricht-Lundborg type in the M
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Anna-Elina Lehesjoki; Carlo Alberto Tassinari; Giuliano Avanzini; Roberto Michel
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Article
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1994
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Springer
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English
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Seven phenotypically homogeneous Mediterranean myoclonus families were studied using DNA markers from the genetically defined EPM1 region on chromosome 21. No recombinations between the disease phenotype and the markers studied were detected. Within the EPM 1 region, the highest lod score value of 5