A novel mutation W388X underlying properdin deficiency in a Finnish family

M Helminen, S Seitsonen, H Jarva, S Meri, IE Järvelä

Research output: Contribution to journalArticleScientificpeer-review

7 Citations (Scopus)
Original languageEnglish
Pages (from-to)445-448
JournalSCANDINAVIAN JOURNAL OF IMMUNOLOGY
Volume75
Issue number4
DOIs
Publication statusPublished - 2012
Publication typeA1 Journal article-refereed

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  • Publication forum level 1

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