Localization of the McLeod locus (XK) within Xp21 by deletion analysis.

The McLeod phenotype is an X-linked, recessive disorder in which the red blood cells demonstrate acanthocytic morphology and weakened antigenicity in the Kell blood group system. The phenotype is associated with a reduction of in vivo red cell survival, but the permanent hemolytic state is usually c...

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Hlavní autoři: Bertelson, C J, Pogo, A O, Chaudhuri, A, Marsh, W L, Redman, C M, Banerjee, D, Symmans, W A, Simon, T, Frey, D, Kunkel, L M
Médium: Artigo
Jazyk:Inglês
Vydáno: 1988
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715185/
https://ncbi.nlm.nih.gov/pubmed/3358422
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