Proximal Dominant Hereditary Motor and Sensory Neuropathy with TFG Mutation: First Case Report from India

Author:

Ansari AfrozF,Jagiasi Kamlesh,Ojha Pawan,Ansari Raahil,Nagendra Shashank,Kharat Sumit

Publisher

Medknow

Subject

Neurology (clinical),Neurology

Reference8 articles.

1. ClinVar: Public archive of relationships among sequence variation and human phenotype;Landrum;Nucleic Acids Res,2014

2. Online Mendelian Inheritance in man (OMIM), a knowledgebase of human genes and genetic disorders;Hamosh;Nucleic Acids Res,2005

3. A new type of hereditary motor and sensory neuropathy linked to chromosome 3;Takashima;Ann Neurol,1997

4. Autosomal dominant hmsn with proximal involvement: New Brazilian cases;Patroclo;Arq Neuropsiquiatr,2009

5. Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot-Marie-Tooth patients with TFG mutation;Khani;Am J Med Genet A,2019

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