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Connection

Peter Pytel to Neuromuscular Junction Diseases

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This is a "connection" page, showing publications Peter Pytel has written about Neuromuscular Junction Diseases.
Peter Pytel
Connection Strength
0.149
Neuromuscular Junction Diseases
  1. Presynaptic congenital myasthenic syndrome with a homozygous sequence variant in LAMA5 combines myopia, facial tics, and failure of neuromuscular transmission. Am J Med Genet A. 2017 Aug; 173(8):2240-2245.
    View in: PubMed
    Score: 0.149
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.