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Connection

Trevor Carmichael to Mutation

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

0,375
  1. Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family. Mol Vis. 2018; 24:407-413.
    View in: PubMed
    Score: 0,134
  2. Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family. BMC Med Genet. 2016 07 20; 17(1):47.
    View in: PubMed
    Score: 0,117
  3. MYOC mutations in black south african patients with primary open-angle glaucoma: genetic testing and cascade screening. Ophthalmic Genet. 2015 Mar; 36(1):31-8.
    View in: PubMed
    Score: 0,104
  4. Myocilin mutations in black South Africans with POAG. Mol Vis. 2011 Apr 27; 17:1064-9.
    View in: PubMed
    Score: 0,020
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.