Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
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Connection

Stephan Ossowski to Spinocerebellar Ataxias

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This is a "connection" page, showing publications Stephan Ossowski has written about Spinocerebellar Ataxias.
Stephan Ossowski
Connection Strength
0,219
Spinocerebellar Ataxias
  1. Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy. Genet Med. 2022 10; 24(10):2079-2090.
    View in: PubMed
    Score: 0,219
Connection Strength

The connection strength for topics 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.
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