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Connection

QIN SUN to Mutation, Missense

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This is a "connection" page, showing publications QIN SUN has written about Mutation, Missense.
QIN SUN
Connection Strength
0.023
Mutation, Missense
  1. Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States. Mol Genet Metab. 2015 Nov; 116(3):139-45.
    View in: PubMed
    Score: 0.023
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.