Polymorphic microsatellites and Wilson disease (WD)

Wilson disease (WD), an autosomal recessive disorder of copper metabolism, has been previously mapped to chromosome 13q. Highly informative PCR-based polymorphic microsatellites closely linked to the WD locus (WND) at 13q14.3, as well as sequence-tagged sites for closely linked loci, are described....

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Bibliografische gegevens
Hoofdauteurs: Stewart, E. A., White, A., Tomfohrde, J., Osborne-Lawrence, S., Prestridge, L., Bonne-Tamir, B., Scheinberg, I. H., George-Hyslop, P. St, Giagheddu, M., Kim, J.-W., Seo, J. K., Lo, W. H.-y., Ivanova-Smolenskaya, I. A., Limborska, S. A., Cavalli-Sforza, L. L., Farrer, L. A., Bowcock, A. M.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1993
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Original Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682397/
https://ncbi.nlm.nih.gov/pubmed/8213814
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