DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
LinksClose Window
References
Boaretto F, Cacciavillani M, Mostacciuolo ML. et al.
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotonia.
Muscle Nerve 2015;
52 (04) 688-689
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.