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Assessing the Utility of ColabFold and AlphaMissense in Determining Missense Variant Pathogenicity for Congenital Myasthenic Syndromes

Background/Objectives: Congenital myasthenic syndromes (CMSs) are caused by variants in >30 genes with increasing numbers of variants of unknown significance (VUS) discovered by next-generation sequencing. Establishing VUS pathogenicity requires in vitro studies that slow diagnosis and treatment ini...

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Autores principales: Finlay Ryan-Phillips, Leighann Henehan, Sithara Ramdas, Jacqueline Palace, David Beeson, Yin Yao Dong
Formato: Artigo
Lenguaje:Inglês
Publicado: MDPI AG 2024-11-01
Colección:Biomedicines
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Acceso en línea:https://www.mdpi.com/2227-9059/12/11/2549
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