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Connection

T. Conrad Gilliam to Fibrosis

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This is a "connection" page, showing publications T. Conrad Gilliam has written about Fibrosis.
T. Conrad Gilliam
Connection Strength
0.038
Fibrosis
  1. Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation. Hum Mol Genet. 1999 Sep; 8(9):1665-71.
    View in: PubMed
    Score: 0.038
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.