Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?
- DOI
- 10.1016/s0960-8966(97)00041-2
- Published
- 1997-06-01
- Container
- Neuromuscul Disord
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1016/s0960-8966-97-00041-2,
title = {Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?},
author = {Udd B and Krahe R and Wallgren-Pettersson C and Falck B and Kalimo H.},
year = {1997},
journal = {Neuromuscul Disord},
doi = {10.1016/s0960-8966(97)00041-2},
url = {https://doi.org/10.1016/s0960-8966(97)00041-2}
}RIS
TY - JOUR TI - Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes? AU - Udd B AU - Krahe R AU - Wallgren-Pettersson C AU - Falck B AU - Kalimo H. PY - 1997 JO - Neuromuscul Disord DO - 10.1016/s0960-8966(97)00041-2 UR - https://doi.org/10.1016/s0960-8966(97)00041-2 ER -
APA
B, U., R, K., C, W., B, F., & H., K. (1997). Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?. Neuromuscul Disord. https://doi.org/10.1016/s0960-8966(97)00041-2
Source records
- europe-pmc · retrieved 2026-09-26T17:15:12.086Z