#frontiersingenetics — Public Fediverse posts
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Incidentally, in our latest article in #FrontiersInGenetics we discuss the "Opportunities and challenges for newborn screening and early diagnosis of rare diseases in Latin America" including the opportunity to implement #GenomicSequencing as an add-on to current NBS programs to provide accurate diagnoses for patients living with #RareDiseases in #LATAM #GenomicEquity
https://www.frontiersin.org/articles/10.3389/fgene.2022.1053559/full
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Proud to share our latest article on "Opportunities & Challenges for Newborn Screening and Early Diagnosis of Rare Diseases in Latin America" published today in #FrontiersInGenetics
This article is the product of careful review, deep discussion & insightful consensus on the current state and opportunities of newborn screening & early diagnosis approaches in Latin America for the better & accurate diagnosis of #RareDisease patients in #LATAM #ERCAL
https://www.frontiersin.org/articles/10.3389/fgene.2022.1053559/full