R Scofield to Homozygote
This is a "connection" page, showing publications R Scofield has written about Homozygote.
Connection Strength
0.138
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Prolidase deficiency and the biochemical assays used in its diagnosis. Anal Biochem. 2006 Feb 15; 349(2):165-75.
Score: 0.063
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Loss-of-function variants in SAT1 cause X-linked childhood-onset systemic lupus erythematosus. Ann Rheum Dis. 2022 Dec; 81(12):1712-1721.
Score: 0.050
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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.
Score: 0.025