Connection

Bradley Schulte to Mutation

This is a "connection" page, showing publications Bradley Schulte has written about Mutation.
Connection Strength

0.091
  1. Dystroglycan expression in the mouse cochlea. Hear Res. 2003 Mar; 177(1-2):12-20.
    View in: PubMed
    Score: 0.037
  2. Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes. BMC Med Genomics. 2018 Sep 04; 11(1):77.
    View in: PubMed
    Score: 0.027
  3. Expression of alpha and beta subunit isoforms of Na,K-ATPase in the mouse inner ear and changes with mutations at the Wv or Sld loci. Hear Res. 1994 Jul; 78(1):65-76.
    View in: PubMed
    Score: 0.020
  4. Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice. Hum Mol Genet. 1999 Aug; 8(8):1579-84.
    View in: PubMed
    Score: 0.007
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.