Characterization of a group unrelated patients with arthrogryposis multiplex congenita
Objective: Arthrogryposis multiplex congenita is a relatively rare neuromuscular syndrome, with a prevalence of 1:3000-5000 newborns. In this study, the authors describe the clinical features of a group of 50 unrelated Mexican patients with arthrogryposis multiplex congenita. Methods: Patients were...
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| Main Authors: | , , , , |
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| Formato: | Libro |
| Publicado: |
Elsevier,
2016-01-01T00:00:00Z.
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| Subjects: | |
| Acceso en liña: | Connect to this object online. |
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Internet
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| Número de Clasificación: |
A1234.567 |
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| Copia 1 | Dispoñible |