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Connection

Benjamin Glick to Arthrogryposis

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This is a "connection" page, showing publications Benjamin Glick has written about Arthrogryposis.
Benjamin Glick
Connection Strength
0.077
Arthrogryposis
  1. Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis. Hum Mol Genet. 2009 Sep 15; 18(18):3462-9.
    View in: PubMed
    Score: 0.077
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.