INVESTIGACIÓN EN ENFERMEDADES RARAS
Maastricht University Medical Centre
Maastricht, HolandaPublicaciones en colaboración con investigadores/as de Maastricht University Medical Centre (1)
2022
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Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants
Genetics in Medicine, Vol. 24, Núm. 11, pp. 2351-2366