Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population

BACKGROUND: Homozygosity or compound heterozygosity for coding region mutations of the hemojuvelin gene (HJV) in whites is a cause of early age-of-onset iron overload (juvenile hemochromatosis), and of hemochromatosis phenotypes in some young or middle-aged adults. HJV coding region mutations have a...

Descripción completa

Detalles Bibliográficos
Autores principales: Barton, James C, Rivers, Charles A, Niyongere, Sandrine, Bohannon, Sean B, Acton, Ronald T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC544351/
https://www.ncbi.nlm.nih.gov/pubmed/15610558
http://dx.doi.org/10.1186/1471-2350-5-29

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC544351/
https://www.ncbi.nlm.nih.gov/pubmed/15610558
http://dx.doi.org/10.1186/1471-2350-5-29

Ejemplares similares