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.
DOI: https://doi.org/10.15844/pedneurbriefs-12-9-6 | Journal eISSN: 2166-6482
Language: English
Page range: 69 - 69
Published on: Sep 1, 1998
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 1998 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.