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Connection

Angela Lager to Genome, Human

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This is a "connection" page, showing publications Angela Lager has written about Genome, Human.
Angela Lager
Connection Strength
0.113
Genome, Human
  1. Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene. Hum Mutat. 2018 11; 39(11):1569-1580.
    View in: PubMed
    Score: 0.113
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.