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Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations
2011
105 citations
Journal Article
green Open Access
Field-Weighted Citation Impact:
2.47
Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations | Researchclopedia
Dr. Behçet Uz Çocuk Hastalıkları Hastanesi
Lennart Truedsson
·
Lund University
Peter Garred
·
Rigshospitalet