Population
44-member pedigree segregating Rippling muscle disease as an autosomal dominant trait, and two previously…
Design
Other
Authors
Loading...
May guide genetic counseling in rippling muscle disease families; leaves open specific gene identification at 1q41.
Rippling muscle disease exhibits genetic heterogeneity, with one responsible gene localized to chromosome 1q41.
Stephan et al. (1994) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: