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Schwartz–Jampel syndrome
Schwartz–Jampel syndrome is a very rare congenital myotonic syndrome with typical phenotypic and electrophysiological features. Diagnosis is made by awareness into the typical phenotypic characters.
Gardado en:
| Publicado en: | J Pediatr Neurosci |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4489067/ https://ncbi.nlm.nih.gov/pubmed/26167227 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.159202 |
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