Document Detail


Autosomal recessive oculopharyngeal muscular dystrophy.
MedLine Citation:
PMID:  1219124     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
K Fried; A Arlozorov; R Spira
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Journal of medical genetics     Volume:  12     ISSN:  0022-2593     ISO Abbreviation:  J. Med. Genet.     Publication Date:  1975 Dec 
Date Detail:
Created Date:  1976-05-25     Completed Date:  1976-05-25     Revised Date:  2010-09-07    
Medline Journal Info:
Nlm Unique ID:  2985087R     Medline TA:  J Med Genet     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  416-8     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Blepharoptosis / genetics
Female
Genes, Recessive*
Humans
Middle Aged
Muscular Dystrophies / genetics*
Oculomotor Muscles*
Pharynx*
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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