Connection

LISA SATTER to Congenital Disorders of Glycosylation

This is a "connection" page, showing publications LISA SATTER has written about Congenital Disorders of Glycosylation.
  1. Expansion of the clinical phenotype of GALE deficiency. Am J Med Genet A. 2021 10; 185(10):3118-3121.
    View in: PubMed
    Score: 0.176
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.