Post-mortem examination in deceased individuals with infantile-onset Pompe disease reveals glycogen accumulation in a wide range of tissues

Authors

L. Pena
P. Kishnani
A. D. Proia

Document Type

Presentation

Date of Publication

2014

Event

American College of Medical Genetics Annual Meeting

Recommended Citation

Pena, L.; Kishnani, P.; and Proia, A. D., "Post-mortem examination in deceased individuals with infantile-onset Pompe disease reveals glycogen accumulation in a wide range of tissues" (2014). Osteopathic Medicine, Jerry M. Wallace School of. 424.
https://cufind.campbell.edu/medicine_school/424