Genome Sequencing for Newborn Screening-An Effective Approach for Tackling Rare Diseases

JAMA Netw Open. 2023 Sep 5;6(9):e2331141. doi: 10.1001/jamanetworkopen.2023.31141.

Authors

Shan Jiang^{1

2}, Haiyin Wang¹, Yuanyuan Gu²

Affiliations

¹ Shanghai Health Development Research Centre, Shanghai, China.
² Macquarie University Centre for the Health Economy, Macquarie Business School and Australian Institute of Health Innovation, Macquarie University, Sydney, New South Wales, Australia.

PMID: 37656463
DOI: 10.1001/jamanetworkopen.2023.31141

No abstract available

Publication types

Comment

MeSH terms

Humans
Infant, Newborn
Neonatal Screening*
Rare Diseases* / diagnosis
Rare Diseases* / genetics