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Connection

Isaac Skromne to Polymorphism, Single Nucleotide

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This is a "connection" page, showing publications Isaac Skromne has written about Polymorphism, Single Nucleotide.
Isaac Skromne
Connection Strength
0.014
Polymorphism, Single Nucleotide
  1. Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss. Am J Hum Genet. 2012 11 02; 91(5):872-82.
    View in: PubMed
    Score: 0.014
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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.