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Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis

F. Petry; A. Izzet Berkel; Michael Loos
Human Genetics · Vol. 100, Issue 1 · pp. 51-56 · 1997
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date1997-06-19
Publication Year1997
Volume100
Issue1
Pages51-56
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s004390050464

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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