'Double trouble': Diagnostic challenges in Duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasia

Authors

Sandra Donkervoort, National Institutes of Health
Alice Schindler, National Institutes of Health
Carolina Tesi-Rocha, George Washington University
Allison Schreiber, Johns Hopkins University
Meganne E. Leach, National Institutes of Health
Jahannaz Dastgir, National Institutes of Health
Ying Hu, National Institutes of Health
Ami Mankodi, National Institutes of Health
Kathryn R. Wagner, Johns Hopkins University
Neil R. Friedman, Cleveland Clinic
Carsten G. Bonnemann, National Institutes of Health

Document Type

Journal Article

Publication Date

12-2013

Journal

Neuromuscular Disorders

Volume

Volume 23, Issue 12

Inclusive Pages

955-961

APA Citation

Donkervoort, S., Schindler, A., Tesi-Rocha, C., Schreiber, A., Leach, M. E., Dastgir, J., Hu, Y., Mankodi, A., Wagner, K.R., Friedman, N.R., Bönnemann, C. G. (2013). 'Double trouble': Diagnostic challenges in duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasia. Neuromuscular Disorders, 23(12), 955-961.

Peer Reviewed

1