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Familial Creutzfeldt-Jakob Disease Cluster Among an African American Family
Familial Creutzfeldt-Jakob disease (fCJD) results from inheritance of mutations in the prion protein gene. Confirming fCJD diagnosis is essential for informing persons of their potential hereditary risk and for genetic counseling to support personal decisions for genetic testing and family planning....
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| Publicado no: | J Public Health Manag Pract |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6947528/ https://ncbi.nlm.nih.gov/pubmed/27997483 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/PHH.0000000000000464 |
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