Marianne Schwartz
Department of Clinical Genetics
National University Hospital
Rigshospitalet
Copenhagen
Denmark
Name/email consistency: high
- Deletion of exon 16 of the dystrophin gene is not associated with disease. Schwartz, M., Dunø, M., Palle, A.L., Krag, T., Vissing, J. Hum. Mutat. (2007)
- LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype. Schwartz, M., Hertz, J.M., Sveen, M.L., Vissing, J. Neurology (2005)