NIH and collaborators identify the genomic cause for Carey-Fineman-Ziter syndrome

(NIH/National Human Genome Research Institute) An international team of researchers has identified genomic mutations 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.

from EurekAlert! - Social and Behavioral Science http://ift.tt/2tV3RG0