A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies.
- DOI
- 10.1016/0960-8966(95)00040-2
- Published
- 1996 May
- Container
- Neuromuscular disorders : NMD
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/0960-8966-95-00040-2,
title = {A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies.},
author = {Meola G and Sansone V and Radice S and Skradski S and Ptacek L},
year = {1996},
journal = {Neuromuscular disorders : NMD},
doi = {10.1016/0960-8966(95)00040-2},
url = {https://doi.org/10.1016/0960-8966(95)00040-2}
}RIS
TY - JOUR TI - A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies. AU - Meola G AU - Sansone V AU - Radice S AU - Skradski S AU - Ptacek L PY - 1996 JO - Neuromuscular disorders : NMD DO - 10.1016/0960-8966(95)00040-2 UR - https://doi.org/10.1016/0960-8966(95)00040-2 ER -
APA
G, M., V, S., S, R., S, S., & L, P. (1996). A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies.. Neuromuscular disorders : NMD. https://doi.org/10.1016/0960-8966(95)00040-2
Source records
- pubmed · retrieved 2026-09-27T10:53:00.347Z