Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy (2019)
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/10.18154/rwth-conv-240896
Publication URI: https://publications.rwth-aachen.de/record/783941
Type: Other