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Connection

James Reid Gilmore to Transferrin

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This is a "connection" page, showing publications James Reid Gilmore has written about Transferrin.
James Reid Gilmore
Connection Strength
0.026
Transferrin
  1. Shrimal S, Ng BG, Losfeld ME, Gilmore R, Freeze HH. Mutations in STT3A and STT3B cause two congenital disorders of glycosylation. Hum Mol Genet. 2013 Nov 15; 22(22):4638-45.
    View in: PubMed
    Score: 0.026
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.