Abstract
Mammalian small heat-shock proteins are suspected to have a role in neuromuscular function. Two new studies provide evidence for the association of mutations in two of these proteins, HSP22 and HSP27, with human neuromuscular disorders.
Cite
CITATION STYLE
APA
Benndorf, R., & Welsh, M. J. (2004, June). Shocking degeneration. Nature Genetics. https://doi.org/10.1038/ng0604-547
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