Congenital myasthenic syndrome caused by a frameshift insertion mutation in GFPT1

OBJECTIVE: Description of a new variant of the glutamine-fructose-6-phosphate transaminase 1 (GFPT1) gene causing congenital myasthenic syndrome (CMS) in 3 children from 2 unrelated families. METHODS: Muscle biopsies, EMG, and whole-exome sequencing were performed. RESULTS: All 3 patients presented...

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Detalles Bibliográficos
Autores principales: Szelinger, Szabolcs, Krate, Jonida, Ramsey, Keri, Strom, Samuel P., Shieh, Perry B., Lee, Hane, Belnap, Newell, Balak, Chris, Siniard, Ashley L., Russell, Megan, Richholt, Ryan, Both, Matt De, Claasen, Ana M., Schrauwen, Isabelle, Nelson, Stanley F., Huentelman, Matthew J., Craig, David W., Yang, Samuel P., Moore, Steven A., Sivakumar, Kumaraswamy, Narayanan, Vinodh, Rangasamy, Sampathkumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357421/
https://www.ncbi.nlm.nih.gov/pubmed/32754643
http://dx.doi.org/10.1212/NXG.0000000000000468

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357421/
https://www.ncbi.nlm.nih.gov/pubmed/32754643
http://dx.doi.org/10.1212/NXG.0000000000000468

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