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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Veröffentlicht in:	Npj genomic medicine 2020-11, Vol.5 (1), p.49-49, Article 49
Hauptverfasser:	Kingsmore, Stephen F., Henderson, Audrey, Owen, Mallory J., Clark, Michelle M., Hansen, Christian, Dimmock, David, Chambers, Christina D., Jeliffe-Pawlowski, Laura L., Hobbs, Charlotte
Format:	Artikel
Sprache:	eng
Schlagworte:	692/4017 Babies Bioinformatics Biomedical and Life Sciences Biomedicine Gene Function Gene Therapy Genetic disorders Genetics & Heredity Human Genetics Infant mortality Internal Medicine Life Sciences & Biomedicine Science & Technology
Online-Zugang:	Volltext
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