Helminen, M., Seitsonen, S., Jarva, H., Meri, S., & Järvelä, I. E. (2012). A novel mutation W388X underlying properdin deficiency in a Finnish family.

Helminen, Merja, Sanna Seitsonen, Hanna Jarva, Seppo Meri, e Irma E. Järvelä. A Novel Mutation W388X Underlying Properdin Deficiency in a Finnish Family. 2012.

Helminen, Merja, et al. A Novel Mutation W388X Underlying Properdin Deficiency in a Finnish Family. 2012.