Utilidad de un algoritmo diagnóstico en la hiperferritinemia: presentación de una familia española con hemocromatosis hereditaria y mutación en el gen SLC40A1 / Usefulness of a diagnostic algorithm hyperferritinemia: A case report of a Spanish family with hereditary hemochromatosis and mutation in SLC40A1 gene
Med. clín (Ed. impr.)
; 145(1): 42-43, jul. 2015.
Article
in Spanish
| IBECS
| ID: ibc-138560
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
No disponible
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Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
Iron Overload
/
Epidemiological Monitoring
/
Hemochromatosis
Type of study:
Diagnostic study
/
Prognostic study
/
Screening study
Limits:
Humans
/
Male
Country/Region as subject:
Europa
Language:
Spanish
Journal:
Med. clín (Ed. impr.)
Year:
2015
Document type:
Article
Institution/Affiliation country:
Centro de Investigación Biomédica en Red en Enfermedades Raras/España
/
Hospital Universitario Puerta de Hierro/España
/
Instituto de Investigación Biomédica Puerta de Hierro (IDIPHIM)/España