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Connection

Michael Yaron to Amino Acid Sequence

This is a "connection" page, showing publications Michael Yaron has written about Amino Acid Sequence.

 
Connection Strength
 
 
 
0.012
 
  1. Levartovsky D, Lagziel A, Sperling O, Liberman U, Yaron M, Hosoya T, Ichida K, Peretz H. XDH gene mutation is the underlying cause of classical xanthinuria: a second report. Kidney Int. 2000 Jun; 57(6):2215-20.
    View in: PubMed
    Score: 0.009
  2. Gafni J, Fischel B, Reif R, Yaron M, Pras M. Amyloidotic polyneuropathy in a Jewish family. Evidence for the genetic heterogeneity of the lower limb familial amyloidotic neuropathies. Q J Med. 1985 Apr; 55(216):33-44.
    View in: PubMed
    Score: 0.003
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.

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