Autosomal recessive oculopharyngeal muscular dystrophy.
Open Access
- 1 December 1975
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 12 (4), 416-418
- https://doi.org/10.1136/jmg.12.4.416
Abstract
Oculopharyngeal muscular dystrophy is known as a rare automsomal dominant disease. A family is reported suggesting that there may be genetic heterogeneity in oculopharyngeal muscular dystrophy and that in some families the mode of inheritance may be autosomal recessive.This publication has 10 references indexed in Scilit:
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- Oculopharyngeal muscular dystrophy.1971
- [Late hereditary oculopharyngeal myopathy].1971
- OCULOPHARYNGEAL MUSCULAR DYSTROPHYActa Neurologica Scandinavica, 1969
- Ocular myopathy with dysphagiaNeurology, 1965
- Muscular DystrophyArchives of Neurology, 1964
- Sphincter Involvement in Ocular MyopathyArchives of Neurology, 1964
- Oculopharyngeal Muscular DystrophyNew England Journal of Medicine, 1962
- PROGRESSIVE DYSTROPHY OF THE EXTERNAL OCULAR MUSCLESBrain, 1951