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Connection

BENJAMIN SHNEIDER to Sequence Deletion

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This is a "connection" page, showing publications BENJAMIN SHNEIDER has written about Sequence Deletion.
BENJAMIN SHNEIDER
Connection Strength
0.010
Sequence Deletion
  1. A novel intronic mutation results in the use of a cryptic splice acceptor site within the coding region of UGT1A1, causing Crigler-Najjar syndrome type 1. Mol Genet Metab. 2002 Feb; 75(2):134-42.
    View in: PubMed
    Score: 0.010
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.