Tiny DNA Deletion Including SNORD116 Gene Causes PWS-Like Disease, Case Study Shows
Loss of a region on chromosome 15 that involves the SNORD116 gene leads to the development of Prader-Willi syndrome (PWS)-like disease, suggesting that missing the gene is enough to cause the key characteristics of PWS, according to a case study. The study, “Prader–Willi-Like Phenotype Caused by…