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Connection

Luca Vricella to Mutation, Missense

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This is a "connection" page, showing publications Luca Vricella has written about Mutation, Missense.
Luca Vricella
Connection Strength
0.037
Mutation, Missense
  1. First evidence of maternally inherited mosaicism in TGFBR1 and subtle primary myocardial changes in Loeys-Dietz syndrome: a case report. BMC Med Genet. 2018 09 15; 19(1):170.
    View in: PubMed
    Score: 0.037
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.