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 https://t.co/crXO9a8fWz https://t.co/3KjBYleLDb
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New Research: 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: Objectives Amyotrophic lateral sclerosis (ALS) is a… https://t.co/i6y0MhH8Zy #
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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 https://t.co/VziFsrFsvh