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Connection

FERNANDO SCAGLIA to Optic Atrophy, Hereditary, Leber

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This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Optic Atrophy, Hereditary, Leber.
FERNANDO SCAGLIA
Connection Strength
0.376
Optic Atrophy, Hereditary, Leber
  1. Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation. Mol Genet Metab. 2011 Jun; 103(2):153-60.
    View in: PubMed
    Score: 0.376
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.