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Connection

WILLIAM CRAIGEN to Phenylalanine Hydroxylase

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This is a "connection" page, showing publications WILLIAM CRAIGEN has written about Phenylalanine Hydroxylase.
WILLIAM CRAIGEN
Connection Strength
0.155
Phenylalanine Hydroxylase
  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: 0.155
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.