What is it about?
About variable clinical manifestations of patients that they carry mutations in TFG gene.
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Why is it important?
Identification of a second Iranian HMSN-P pedigree further confirms that HMSN-P is not confined to the Far East.
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This page is a summary of: Identification of novel TFG mutation in HMSN-P pedigree: Emphasis on variable clinical presentations, Journal of the Neurological Sciences, October 2016, Elsevier,
DOI: 10.1016/j.jns.2016.08.035.
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