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Connection

FERNANDO SCAGLIA to Enoyl-CoA Hydratase

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This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Enoyl-CoA Hydratase.
FERNANDO SCAGLIA
Connection Strength
0.664
Enoyl-CoA Hydratase
  1. Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short-chain enoyl-CoA hydratase deficiency. Am J Med Genet A. 2019 05; 179(5):803-807.
    View in: PubMed
    Score: 0.664
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.