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New Study Shows Comprehensive Genomic Evidence is Critical for Calculating Rare Disease Prevalence
Ann Arbor, Michigan (PRWEB) December 15, 2022 Genomenon, Inc., an AI-driven genomics company, today announced the publication of a paper in the Orphanet
Inozyme pharma
Mark kiel
Catherine nester
National institutes of health
University children hospital
Genomenon inc
Vice president
Patient strategies
Orphanet journal
Rare diseases
National institutes
University children
Genomenon chief scientific officer
Genetic prevalence using
Comprehensive literature review
Press release
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