Congenital Myasthenic Syndrome with Agrin Mutations
Investigators at Newcastle University, UK, and Hopitaux de Paris, France, report 5 patients from 3 unrelated families with a strikingly homogeneous clinical entity combining congenital myasthenia with distal muscle weakness and atrophy resembling a distal myopathy.
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Pediatric Neurology Briefs Publishers
2014-10-01
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| Series: | Pediatric Neurology Briefs |
| Subjects: | |
| Online Access: | https://www.pediatricneurologybriefs.com/articles/81 |