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Connection

R Scofield to Homozygote

This is a "connection" page, showing publications R Scofield has written about Homozygote.
Connection Strength

0.138
  1. Prolidase deficiency and the biochemical assays used in its diagnosis. Anal Biochem. 2006 Feb 15; 349(2):165-75.
    View in: PubMed
    Score: 0.063
  2. Loss-of-function variants in SAT1 cause X-linked childhood-onset systemic lupus erythematosus. Ann Rheum Dis. 2022 Dec; 81(12):1712-1721.
    View in: PubMed
    Score: 0.050
  3. Identification of novel coding mutation in C1qA gene in an African-American pedigree with lupus and C1q deficiency. Lupus. 2012 Sep; 21(10):1113-8.
    View in: PubMed
    Score: 0.025
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.