Associated Papers
Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot-Marie-Tooth patients with TFG mutation.
Khani M et al.
American Journal of Medical Genetics. Part A, 2019
Identification of novel TFG mutation in HMSN-P pedigree: Emphasis on variable clinical presentations.
Khani M et al.
Journal of the Neurological Sciences, 2016
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