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Reorganizing the protein space at the Universal Protein Resource (UniProt)
Ongoing and future developments at the Universal Protein Resource
Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis
Phenopolis: an open platform for harmonization and analysis of sequencing and phenotype data
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease