Hereditary Inclusion Body Myopathy
DOI:
https://doi.org/10.15844/pedneurbriefs-12-9-6Keywords:
Hereditary Inclusion Body Myopathy, External Ophthalmoplegia, Myopathic ChangesAbstract
A new familial, autosomal dominant, myopathy and variant of hereditary inclusion body myopathy (HIBM) is described in 19 members of a large Swedish family followed in the Departments of Pediatrics, Genetics, and Pathology, Sahlgrenska University Hospital, Goteborg, Sweden.Published
1998-09-01
Issue
Section
Neuromuscular Disorders
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Copyright (c) 1998 The Author(s)
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