New compound heterozygous variants of the cholinergic receptor nicotinic delta subunit gene in a Chinese male with congenital myasthenic syndrome: A case report

INTRODUCTION: Congenital myasthenic syndromes (CMS) are a group of genetic disorders that stem mostly from molecular defects in nicotinic acetylcholine receptors (AChRs). Defects in the cholinergic receptor nicotinic delta subunit (CHRND) gene can cause a series of myasthenic syndromes. Here, we rep...

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Detalles Bibliográficos
Autores principales: Feng, Huiru, Zhou, Hongyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758131/
https://www.ncbi.nlm.nih.gov/pubmed/29390429
http://dx.doi.org/10.1097/MD.0000000000008981

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758131/
https://www.ncbi.nlm.nih.gov/pubmed/29390429
http://dx.doi.org/10.1097/MD.0000000000008981

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