P.35 Genetic newborn screening and digital technologies to accelerate rare disease diagnosis: The EU-IMI screen4Care project
Ferlini, A., Fortunato, F., Farnè, M., Selvatici, R., Blankart, C., Röttger, R., Kirschner, J., Schenk, J., Zarakowska, K., Zschüntzsch, J., Man, Y., Goodman, L., Gross, E., Garnier, N.
Published in Neuromuscular disorders : NMD (01.10.2022)
Published in Neuromuscular disorders : NMD (01.10.2022)
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