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Connection

Lijun Xia to Genetic Diseases, Inborn

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This is a "connection" page, showing publications Lijun Xia has written about Genetic Diseases, Inborn.
Lijun Xia
Connection Strength
0.155
Genetic Diseases, Inborn
  1. Site-1 protease deficiency causes human skeletal dysplasia due to defective inter-organelle protein trafficking. JCI Insight. 2018 07 26; 3(14).
    View in: PubMed
    Score: 0.155
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.