Response to Grosse et al
- PMID: 37267897
- PMCID: PMC10256999
- DOI: 10.1016/j.ajhg.2023.05.004
Response to Grosse et al
Comment on
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Progress in expanding newborn screening in the United States.Am J Hum Genet. 2023 Jun 1;110(6):1015-1016. doi: 10.1016/j.ajhg.2023.05.002. Am J Hum Genet. 2023. PMID: 37267896 Free PMC article. No abstract available.
References
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- Kingsmore S.F., Smith L.D., Kunard C.M., Bainbridge M., Batalov S., Benson W., Blincow E., Caylor S., Chambers C., Del Angel G., et al. A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases. Am. J. Hum. Genet. 2022;109:1605–1619. - PMC - PubMed
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- Yu T.W., Kingsmore S.F., Green R.C., MacKenzie T., Wasserstein M., Caggana M., Gold N.B., Kennedy A., Kishnani P.S., Might M., et al. Are we prepared to deliver gene-targeted therapies for rare diseases? Am. J. Med. Genet. C Semin. Med. Genet. 2023;193:7–12. - PubMed
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