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Connection

Kelly Stratton to Immunologic Deficiency Syndromes

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This is a "connection" page, showing publications Kelly Stratton has written about Immunologic Deficiency Syndromes.
Kelly Stratton
Connection Strength
0.110
Immunologic Deficiency Syndromes
  1. A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome. PLoS Genet. 2013 Aug; 9(8):e1003695.
    View in: PubMed
    Score: 0.110
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.