Mutation Screening of Charcot-Marie-Tooth Patients in Poland
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Veröffentlicht in: | Annals of the New York Academy of Sciences 1999-10, Vol.883 (1), p.493-496 |
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container_title | Annals of the New York Academy of Sciences |
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creator | KOCHAŃSKI, A. TIMMERMAN, V. JEDRZEJOWSKA, H. RYNIEWICZ, B. LÖFGREN, A. De VRIENDT, E. VAN BROECKHOVEN, C. LATOS-BIELEŃSKA, A. HAUSMANOWA-PETRUSEWICZ, I. |
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doi_str_mv | 10.1111/j.1749-6632.1999.tb08619.x |
format | Article |
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source | Wiley Online Library - AutoHoldings Journals; MEDLINE |
subjects | Charcot-Marie-Tooth Disease - diagnosis Charcot-Marie-Tooth Disease - genetics Chromosome Mapping Chromosomes, Human, Pair 17 Connexins - genetics Female Gap Junction beta-1 Protein Genetic Markers Genetic Testing Humans Male Myelin P0 Protein - genetics Myelin Proteins - genetics Pedigree Poland Polymorphism, Restriction Fragment Length |
title | Mutation Screening of Charcot-Marie-Tooth Patients in Poland |
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