Current and future therapeutic approaches to the congenital myopathies (2017)
Attributed to:
Determining how mutations in actin lead to skeletal muscle weakness
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.5451/unibas-ep62498
Publication URI: https://edoc.unibas.ch/62498/
Type: Other