Novel variant c.92T > G (p.Val31Gly) in the PFN1 gene (ALS18) responsible for a specific phenotype in a large Bulgarian amyotrophic lateral sclerosis pedigree.

MLA

Angelov, Teodor, et al. “Novel Variant c.92T > G (p.Val31Gly) in the PFN1 Gene (ALS18) Responsible for a Specific Phenotype in a Large Bulgarian Amyotrophic Lateral Sclerosis Pedigree.” Frontiers in Neurology, vol. 14, Feb. 2023, p. 1094234. EBSCOhost, https://doi.org/10.3389/fneur.2023.1094234.

APA

Angelov, T., Chamova, T., Atemin, S., Todorov, T., Ormandzhiev, S., Tourtourikov, I., Todorova, A., Devos, D., & Tournev, I. (2023). Novel variant c.92T > G (p.Val31Gly) in the PFN1 gene (ALS18) responsible for a specific phenotype in a large Bulgarian amyotrophic lateral sclerosis pedigree. Frontiers in Neurology, 14, 1094234. https://doi.org/10.3389/fneur.2023.1094234

Chicago

Angelov, Teodor, Teodora Chamova, Slavena Atemin, Tihomir Todorov, Slavko Ormandzhiev, Ivan Tourtourikov, Albena Todorova, David Devos, and Ivailo Tournev. 2023. “Novel Variant c.92T > G (p.Val31Gly) in the PFN1 Gene (ALS18) Responsible for a Specific Phenotype in a Large Bulgarian Amyotrophic Lateral Sclerosis Pedigree.” Frontiers in Neurology 14 (February): 1094234. doi:10.3389/fneur.2023.1094234.