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
Hauptverfasser: Dzieżyc, K, Gromadzka, G, Członkowska, A
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container_issue 7
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container_title Parkinsonism & related disorders
container_volume 17
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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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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