CV Lattes
Universidade de São Paulo (USP). Faculdade de Medicina de Ribeirão Preto (FMRP) (Institutional affiliation from the last research proposal) Birthplace: Brazil
Murilo Marques Veronez in research grants and scholarships supported by FAPESP.
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Hereditary hemochromatosis is the most common genetic disease among individuals with European ancestry. Two mutations, C282Y and H63D in the HFE gene are associated with HH. Approximately 85-90% of patients of European descent with HH are homozygous for C282Y. In Brazil, this percentage is unknown because of the great miscegenation. The objectives of this study are to identify individuals…
| 1 / 1 | Completed scholarships in Brazil |
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