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Insights into extensive deletions around the XK locus associated with McLeod phenotype and characterization of two novel cases
The McLeod phenotype is derived from various forms of XK gene defects that result in the absence of XK protein, and is defined hematologically by the absence of Kx antigen, weakening of Kell system antigens, and red cell acanthocytosis. Individuals with the McLeod phenotype usually develop late-onse...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1931494/ https://ncbi.nlm.nih.gov/pubmed/17300882 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gene.2006.11.023 |
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