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Connection

Samuel Refetoff to Myopathies, Structural, Congenital

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This is a "connection" page, showing publications Samuel Refetoff has written about Myopathies, Structural, Congenital.
Samuel Refetoff
Connection Strength
0.320
Myopathies, Structural, Congenital
  1. A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay. Pediatrics. 2008 Jan; 121(1):e199-202.
    View in: PubMed
    Score: 0.320
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.