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Connection

LINDA KIRBY-KEYSER to Adrenal Hyperplasia, Congenital

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This is a "connection" page, showing publications LINDA KIRBY-KEYSER has written about Adrenal Hyperplasia, Congenital.
LINDA KIRBY-KEYSER
Connection Strength
0.133
Adrenal Hyperplasia, Congenital
  1. E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hum Mutat. 1997; 9(2):181-2.
    View in: PubMed
    Score: 0.133
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.