A novel mutation W388X underlying properdin deficiency in a Finnish family

por Helminen, Merja, Seitsonen, Sanna, Jarva, Hanna, Meri, Seppo, Järvelä, Irma E
Publicado 2012

Molecularly defined adult-type hypolactasia among working age people with reference to milk consumption and gastrointestinal symptoms

por Anthoni, Sari R, Rasinperä, Heli A, Kotamies, Antti J, Komu, Hanna A, Pihlajamäki, Harri K, Kolho, Kaija-Leena, Järvelä, Irma E
Publicado 2007

Multifactor Effects and Evidence of Potential Interaction between Complement Factor H Y402H and LOC387715 A69S in Age-Related Macular Degeneration

por Seitsonen, Sanna P., Onkamo, Päivi, Peng, Gang, Xiong, Momiao, Tommila, Petri V., Ranta, Päivi H., Holopainen, Juha M., Moilanen, Jukka A., Palosaari, Tapani, Kaarniranta, Kai, Meri, Seppo, Immonen, Ilkka R., Järvelä, Irma E.
Publicado 2008