Connection

MICHAEL WANGLER to Sequence Homology, Amino Acid

This is a "connection" page, showing publications MICHAEL WANGLER has written about Sequence Homology, Amino Acid.
  1. Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila. Hum Mol Genet. 2016 05 01; 25(9):1846-56.
    View in: PubMed
    Score: 0.120
  2. TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila. Am J Hum Genet. 2021 09 02; 108(9):1669-1691.
    View in: PubMed
    Score: 0.044
Connection Strength

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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.