The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy
Abstract Objective Oculopharyngeal muscular dystrophy (OPMD) is a late‐onset inherited neuromuscular disorder, with progressive ptosis and dysphagia as common manifestations. To date, OPMD has rarely been reported among East Asians. The present study summarizes the phenotypic and genotypic features...
Salvato in:
| Autori principali: | , , , , , , , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wiley
2023-03-01
|
| Serie: | Annals of Clinical and Translational Neurology |
| Accesso online: | https://doi.org/10.1002/acn3.51733 |
| Tags: |
Nessun Tag, puoi essere il primo ad aggiungerne!!
|