D10.1 – Validated bioinformatics tool
D10.2 – Report on finalization endpoint data extraction from clinical database into NONMEM dataset
D10.3 – Report on the association of novel genomic variants and extreme phenotypes
D10.1 – Validated bioinformatics tool
D10.2 – Report on finalization endpoint data extraction from clinical database into NONMEM dataset
D10.3 – Report on the association of novel genomic variants and extreme phenotypes