Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families.
- DOI
- 10.1016/s0960-8966(00)00123-1
- Published
- 2000 Oct
- Container
- Neuromuscular disorders : NMD
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1016/s0960-8966-00-00123-1,
title = {Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families.},
author = {Ausems MG and ten Berg K and Beemer FA and Wokke JH},
year = {2000},
journal = {Neuromuscular disorders : NMD},
doi = {10.1016/s0960-8966(00)00123-1},
url = {https://doi.org/10.1016/s0960-8966(00)00123-1}
}RIS
TY - JOUR TI - Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families. AU - Ausems MG AU - ten Berg K AU - Beemer FA AU - Wokke JH PY - 2000 JO - Neuromuscular disorders : NMD DO - 10.1016/s0960-8966(00)00123-1 UR - https://doi.org/10.1016/s0960-8966(00)00123-1 ER -
APA
MG, A., K, T. B., FA, B., & JH, W. (2000). Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families.. Neuromuscular disorders : NMD. https://doi.org/10.1016/s0960-8966(00)00123-1
Source records
- pubmed · retrieved 2026-09-27T08:38:14.900Z
- europe-pmc · retrieved 2026-09-27T08:38:14.912Z