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Autor:
Uusimaa, J. (Johanna), Kettunen, J. (Johannes), Varilo, T. (Teppo), Järvelä, I. (Irma), Kallijärvi, J. (Jukka), Kääriäinen, H. (Helena), Laine, M. (Minna), Lapatto, R. (Risto), Myllynen, P. (Päivi), Niinikoski, H. (Harri), Rahikkala, E. (Elisa), Suomalainen, A. (Anu), Tikkanen, R. (Ritva), Tyynismaa, H. (Henna), Vieira, P. (Päivi), Zarybnicky, T. (Tomas), Sipilä, P. (Petra), Kuure, S. (Satu), Hinttala, R. (Reetta)
Isolated populations have been valuable for the discovery of rare monogenic diseases and their causative genetic variants. Finnish disease heritage (FDH) is an example of a group of hereditary monogenic disorders caused by single major, usually autos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2423::ae5f5a49a877a717fdd0e03f166f916e
http://urn.fi/urn:nbn:fi-fe2023070481032
http://urn.fi/urn:nbn:fi-fe2023070481032
