Connection

WILLIAM CRAIGEN to Mitochondrial Encephalomyopathies

This is a "connection" page, showing publications WILLIAM CRAIGEN has written about Mitochondrial Encephalomyopathies.
  1. Expanding the phenotype of SLC25A42-associated mitochondrial encephalomyopathy. Clin Genet. 2018 05; 93(5):1097-1102.
    View in: PubMed
    Score: 0.142
  2. Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance. Am J Hum Genet. 2013 Sep 05; 93(3):471-81.
    View in: PubMed
    Score: 0.104
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.