Protocolo genético en Atención Primaria para enfermedades raras: el síndrome de Wolfram como prototipo

Rare diseases, despite their individual low frequency, affect 7% of the population all combined. Consequently, every primary care practitioner (PCP) will have several of these patients under his care. 80% of rare diseases are genetically determined, which makes genetic counseling fundamental in thes...

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Detalles Bibliográficos
Autores principales: Esteban-Bueno, Gema, Díaz-Anadón, Lucas Ramón, Rodríguez González, Antonio, Navarro Cabrero, Miguel, Berenguel Hernández, Aída María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Artículo Especial
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931343/
https://www.ncbi.nlm.nih.gov/pubmed/35307613
http://dx.doi.org/10.1016/j.aprim.2022.102285

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931343/
https://www.ncbi.nlm.nih.gov/pubmed/35307613
http://dx.doi.org/10.1016/j.aprim.2022.102285

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