Genomic mutations have been identified for Carey-Fineman-Ziter (CFZS) syndrome, a very rare inherited muscle disorder. Findings provide insight into the development of an embryo’s muscles and the regeneration of muscle cells after injury.
Genomic mutations have been identified for Carey-Fineman-Ziter (CFZS) syndrome, a very rare inherited muscle disorder. Findings provide insight into the development of an embryo’s muscles and the regeneration of muscle cells after injury.