C.P.4.09 Dynamin 2 mutations in the pleckstrin homology domain cause severe neonatal centronuclear myopathy
- Resource Type
- Source
- Neuromuscular Disorders. 17:881
- Subject
Pleckstrin homology domain Neurology Pediatrics, Perinatology and Child Health medicine Neurology (clinical) Biology Centronuclear myopathy medicine.disease Genetics (clinical) Dynamin Cell biology - Language
- ISSN
- 0960-8966