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A novel TFG variant of uncertain significance in amyotrophic lateral sclerosis: A case report and review of literature
INTRODUCTION: Amyotrophic lateral sclerosis is a neurodegenerative disease with wide variation of genetics associated with it. Among the different genes described, mutation in TFG is a rare finding in amyotrophic lateral sclerosis. CASE PRESENTATION: A 35 years old right-handed male presenting with...
Autores principales: | Dhakal, Bishal, Sapkota, Sachin, Parajuli, Aakriti, Khadka, Bibek, Subedi, Binaya, Paudel, Raju, Thapa, Rohit, Rimal, Sabin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793128/ https://www.ncbi.nlm.nih.gov/pubmed/36582889 http://dx.doi.org/10.1016/j.amsu.2022.104840 |
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