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...

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Detalles Bibliográficos
Autores principales: Dhakal, Bishal, Sapkota, Sachin, Parajuli, Aakriti, Khadka, Bibek, Subedi, Binaya, Paudel, Raju, Thapa, Rohit, Rimal, Sabin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
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

Internet

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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