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Connection

FERNANDO SCAGLIA to Malabsorption Syndromes

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This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Malabsorption Syndromes.
FERNANDO SCAGLIA
Connection Strength
0.105
Malabsorption Syndromes
  1. A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption. Gene. 2013 Sep 25; 527(2):673-4.
    View in: PubMed
    Score: 0.105
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.