Wilson’s disease in consecutive generations of one family
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Veröffentlicht in: | Parkinsonism & related disorders 2011-08, Vol.17 (7), p.577-578 |
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container_title | Parkinsonism & related disorders |
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creator | Dzieżyc, K Gromadzka, G Członkowska, A |
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doi_str_mv | 10.1016/j.parkreldis.2011.04.013 |
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source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Adenosine Triphosphatases - genetics Cation Transport Proteins - genetics Ceruloplasmin - metabolism Consecutive generations Copper-transporting ATPases DNA Mutational Analysis Family Female Hepatolenticular Degeneration - genetics Humans Male Neurology p.H1069Q mutation Pedigree Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Wilson’s disease Wilson’s disease carrier Young Adult |
title | Wilson’s disease in consecutive generations of one family |
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