Hereditary neuromuscular diseases. Part 1. Muscular dystrophies: dystrophinopathy emerinopathy and facio-scapulo-humeral forms
Author:
Affiliation:
1. Department of Neurology First Pavlov State Medical University; Department of neuromuscular diseases, City hospital 2
2. Department of Neurology First Pavlov State Medical University
Publisher
Medical Informational Agency Publishers
Subject
Psychiatry and Mental health,Neurology (clinical),Neurology
Reference48 articles.
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3. Upadhyaya M, Maynard J., Rogers MT., Lunt P.W., Jardine P. Ravine D., and Harper P.S. Improved molecular diagnostic of FSHD. J. Med Genet. 1997;34(6):476-479.
4. Monaco A.P., Bertelson C.J., Liechti-Gallati S., Moser H., Kunkel L.M. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics. 1988:2(1):90-95.
5. Nicholson L.V., Davison K., Johnson M.A., Slater C.R., Young C., Bhattacharya S., Gardner-Medwin D., Harris J.B. Dystrophin in skeletal muscle. Immunoreactivity in patients with Xp21 muscular dystrophy. J. Neurol. Sci 1989;94(1-3):137-146.
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