Fig. 1From: Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case reportA homozygous mutation of the c.278G > T(p.G93V) of the HINT1 gene was identified in the proband and marked with arrow. The same heterozygous variant was found in the patient’s father, mother, and brotherBack to article page