Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing

Understanding causes of infant mortality shapes public health policy and prioritizes diseases for investments in surveillance, intervention and medical research. Rapid genomic sequencing has created a novel opportunity to decrease infant mortality associated with treatable genetic diseases. Herein,...

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Detalles Bibliográficos
Autores principales: Kingsmore, Stephen F., Henderson, Audrey, Owen, Mallory J., Clark, Michelle M., Hansen, Christian, Dimmock, David, Chambers, Christina D., Jeliffe-Pawlowski, Laura L., Hobbs, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608690/
https://www.ncbi.nlm.nih.gov/pubmed/33154820
http://dx.doi.org/10.1038/s41525-020-00155-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608690/
https://www.ncbi.nlm.nih.gov/pubmed/33154820
http://dx.doi.org/10.1038/s41525-020-00155-8

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