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Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.

McLeod syndrome, characterized by acanthocytosis and the absence of a red-blood-cell Kell antigen (Kx), is a multisystem disorder involving a late-onset myopathy, splenomegaly, and neurological defects. The locus for this syndrome has been mapped, by deletion analysis, to a region between the loci f...

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Detalhes bibliográficos
Main Authors: Ho, M F, Monaco, A P, Blonden, L A, van Ommen, G J, Affara, N A, Ferguson-Smith, M A, Lehrach, H
Formato: Artigo
Idioma:Inglês
Publicado em: 1992
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682457/
https://ncbi.nlm.nih.gov/pubmed/1734714
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