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Connection

Michael Cartwright to Hereditary Sensory and Motor Neuropathy

This is a "connection" page, showing publications Michael Cartwright has written about Hereditary Sensory and Motor Neuropathy.
  1. Castoro R, Caress JB, Li J, Cartwright MS. Arg953* mutation in Periaxin causes CMT4F without nerve hypertrophy on ultrasound imaging: A case report and review of the literature. Clin Neurophysiol. 2023 Mar; 147:14-16.
    View in: PubMed
    Score: 0.901
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.