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Combination of factor H mutation and properdin deficiency causes severe C3 glomerulonephritis

eagle-i ID

http://eagle-i.itmat.upenn.edu/i/0000013e-5822-980e-2f2e-ad3380000000

Resource Type

  1. Journal article

Properties

  1. Used by
    Wen-Chao Song Laboratory
  2. PubMed ID
    23204401
 
RDFRDF
 
Inferred Types from the eagle-i Ontology (What is an ontology?)
Provenance Metadata About This Resource Record
  1. workflow state
    Published
  2. contributor
    fcoldren
  3. created
    2013-04-29T19:31:42.589-04:00
  4. creator
    fcoldren
  5. modified
    2013-06-05T16:02:56.437-04:00
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