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Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen
BACKGROUND: The phenotypic heterogeneity of sickle cell disease is likely the result of multiple genetic factors and their interaction with the sickle mutation. High transcranial doppler (TCD) velocities define a subgroup of children with sickle cell disease who are at increased risk for developing...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | en |
| Publicado em: |
BioMed Central
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC183831/ https://ncbi.nlm.nih.gov/pubmed/12871600 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-4-6 |
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