Published 1998 | Version v1.0.0
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Hereditary Inclusion Body Myopathy

Abstract

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.

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PNB-12-69-a

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Created
1998
When the item was originally created.