Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33.

Familial eosinophilia (FE) is an autosomal dominant disorder characterized by peripheral hypereosinophilia of unidentifiable cause with or without other organ involvement. To localize the gene for FE, we performed a genomewide search in a large U.S. kindred, using 312 different polymorphic markers....

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Detalhes bibliográficos
Main Authors: Rioux, J D, Stone, V A, Daly, M J, Cargill, M, Green, T, Nguyen, H, Nutman, T, Zimmerman, P A, Tucker, M A, Hudson, T, Goldstein, A M, Lander, E, Lin, A Y
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377485/
https://ncbi.nlm.nih.gov/pubmed/9758611
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