| Literature DB >> 2703844 |
W J Cumming1, F Kristmundsdottir, M Mahon.
Abstract
Autosomal dominant inheritance of an unusual muscle disease is reported in a family. The pathological appearance, of regularly arranged markedly atrophic muscle fibres without other evidence of disturbed innervation, are similar in each case. However, the onset of the disease, its distribution and its progression has varied within the family.Entities:
Mesh：
Year: 1989 PMID： 2703844 PMCID： PMC1032518 DOI： 10.1136/jnnp.52.2.266
Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN： 0022-3050 Impact factor: 10.154