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Connection

Alexandra Dumitrescu to Myopathies, Structural, Congenital

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This is a "connection" page, showing publications Alexandra Dumitrescu has written about Myopathies, Structural, Congenital.
Alexandra Dumitrescu
Connection Strength
0.073
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: 0.073
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.