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Polymorphic short tandem repeats for PCR-based diagnosis of the Charcot-Marie-Tooth 1A duplication in Ukraine

Charcot-Marie-Tooth neuropathy (CMT) is one of the most common hereditary disorders, affecting 1 : 2500 individuals. The major mutation – microduplication of 1.4 megabases in 17р11.2 region, which is responsible for 68–90 % of cases of CMT1, results in CMT1A. In the present article we provide the po...

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Bibliographic Details
Main Authors: Hryshchenko, N.V., Kravchenko, S.A., Livshits, L.A.
Format: Article
Language:English
Published: Інститут клітинної біології та генетичної інженерії НАН України 2005
Series:Цитология и генетика
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Online Access:http://dspace.nbuv.gov.ua/handle/123456789/126776
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