An international research team identified the cause of a rare muscle disease. According to these findings, a single spontaneously occurring mutation results in the muscle cells no longer being able to correctly break down defective proteins. The condition causes severe heart failure in children, accompanied by skeletal and respiratory muscle damage. The study also highlights experimental approaches for potential treatment. Whether this hope will be fulfilled, however, will only become clear in a few years.
from Top Health News -- ScienceDaily https://ift.tt/3zrYOvl
No comments:
Post a Comment