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.
Connection Strength
0.884
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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.
Score: 0.884