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Bratisl Lek Listy ; 101(1): 14-7, 2000.
Article in Slovak | MEDLINE | ID: mdl-10824406

ABSTRACT

Authors present a clinical symptoms recapitulation of the most important monogenic hereditary neuromuscular diseases, their molecular-genetic causes and the possibilities of diagnostic on the level of DNA analysis. Low detectability of these pathologic states in Slovak republic is stressed and possible causes of this state are analyzed. (Ref. 10.)


Subject(s)
Huntington Disease/diagnosis , Muscular Atrophy, Spinal/diagnosis , Muscular Dystrophies/diagnosis , Humans , Huntington Disease/genetics , Muscular Atrophy, Spinal/genetics , Muscular Dystrophies/genetics , Slovakia
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