Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita)
Year: 1993
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/ng0493-305
Institutions: Vanderbilt University, University Hospital
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2086734513
