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Connection

Willard W. Sharp to Optic Atrophy, Autosomal Dominant

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This is a "connection" page, showing publications Willard W. Sharp has written about Optic Atrophy, Autosomal Dominant.
Willard W. Sharp
Connection Strength
0.028
Optic Atrophy, Autosomal Dominant
  1. PGC1a-mediated mitofusin-2 deficiency in female rats and humans with pulmonary arterial hypertension. Am J Respir Crit Care Med. 2013 Apr 15; 187(8):865-78.
    View in: PubMed
    Score: 0.028
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.