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Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project.

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Bibliographic Details
Title: Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project.
Authors: Ferlini, Alessandra1 (AUTHOR) fla@unife.it, Gross, Edith Sky2 (AUTHOR), Garnier, Nicolas3 (AUTHOR), Berghout, Joanne (AUTHOR), Zygmunt, Aldona (AUTHOR), Singh, Deependra (AUTHOR), Huang, Kui A. (AUTHOR), Kantz, Waltraud (AUTHOR), Blankart, Carl Rudolf (AUTHOR), Gillner, Sandra (AUTHOR), Zhao, Jiawei (AUTHOR), Roettger, Richard (AUTHOR), Saier, Christina (AUTHOR), Kirschner, Jan (AUTHOR), Schenk, Joern (AUTHOR), Atkins, Leon (AUTHOR), Ryan, Nuala (AUTHOR), Zarakowska, Kaja (AUTHOR), Zschüntzsch, Jana (AUTHOR), Zuccolo, Michela (AUTHOR)
Source: Orphanet Journal of Rare Diseases. 10/4/2023, Vol. 18 Issue 1, p1-4. 4p.
Database: Academic Search Ultimate
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Description
ISSN:17501172
DOI:10.1186/s13023-023-02916-x