Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3
This work was supported by the grant CIVP16A1857 “Ayudas a proyectos de Investigacion en Ciencias de la Vida” from Ramon Areces Private Foundation and grant SAF2012-40106 from Ministry of Economy and Competitiveness (MINECO) to M.S. M.S. held a research contract under the Ramon y Cajal program from...
| Autores: | , , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2015 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:20.500.12328/3090 |
| Acceso en línea: | http://hdl.handle.net/20.500.12328/3090 https://dx.doi.org/10.1002/mgg3.136 |
| Access Level: | acceso abierto |
| Palabra clave: | Mutacions Transferrina-2 Hemocromatosi hereditària tipus 3 Mutaciones Hemocromatosis hereditaria tipo 3 Mutations Transferrin-2 Hereditary hemochromatosis type 3 57 |
| Sumario: | This work was supported by the grant CIVP16A1857 “Ayudas a proyectos de Investigacion en Ciencias de la Vida” from Ramon Areces Private Foundation and grant SAF2012-40106 from Ministry of Economy and Competitiveness (MINECO) to M.S. M.S. held a research contract under the Ramon y Cajal program from the Spanish Ministry of Science and Innovation (RYC-2008-02352). M.Shv. held a long-term postdoctoral fellowship from FEBS (Federation of European Biochemical Societies). J.A. held a technician support contract under the “Contratos de Tecnicos de apoyo a la investigacion en el SNS” program from the “Instituto de Salud Carlos III”, Spanish Health Program (CA10/01114). |
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