DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Rauchenzauner M, Frühwirth M, Hecht M, Kofler M, Witsch-Baumgartner M, Fauth C.
A novel variant in the HINT1 gene in a girl with autosomal recessive axonal neuropathy with neuromyotonia: thorough neurological examination gives the clue.
Neuropediatrics 2016;
47 (02) 119-122
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