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Mot de passe oublié? Découvrez toutes les informations sur le Groupe Findis.
Mot de passe oublié? Découvrez toutes les informations sur le Groupe Findis.
Is a centralized resource for cross-referenced information on disease mutations enriched in the Finnish population. FinDis provides up-to-date information on the 36 monogenic diseases belonging to the Finnish disease heritage. Prevalence or incidence and a short description of clinical symptoms. Genetic locus and a molecular description for identified mutations. Disease allele frequencies typically reported for Finnish mutations. Read About the FinDis project.