Familial neuromuscular disease with “myotubes“
- 23 April 1974
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 5 (4), 327-337
- https://doi.org/10.1111/j.1399-0004.1974.tb01702.x
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Centronuclear Myopathy With Type I Fiber Atrophy and "Myotubes"Archives of Neurology, 1970
- Type I muscle fibre atrophy and central nuclei: A rare familial neuromuscular diseaseJournal of the Neurological Sciences, 1970
- Neuromuscular disease with type I fiber atrophy, central nuclei, and myotube‐like structuresNeurology, 1969
- Myotubular myopathyJournal of the Neurological Sciences, 1969
- Myotubular, centronuclear or peri-centronuclear myopathy?Journal of the Neurological Sciences, 1969
- Cerebral Influence on Muscle Fiber TypingArchives of Neurology, 1969
- Hurler and Hunter Syndromes: Mutual Correction of the Defect in Cultured FibroblastsScience, 1968
- Type I Fiber Hypotrophy and Central NucleiArchives of Neurology, 1968
- Centronuclear MyopathyEuropean Neurology, 1968
- The B fiber of human fetal skeletal muscleNeurology, 1963