56.0
David E. Cervantes‐Barragán
Pemex (Mexico)
David E. Cervantes‐Barragán has made significant contributions to various fields of study, including genetics, molecular biology, and pediatric medicine. Their research focuses on understanding rare genetic disorders, such as pigmentary mosaicism, mosaic trisomy 12, Andersen-Tawil syndrome, and Setleis syndrome. Through their studies, Cervantes‐Barragán has shed light on the genetic basis of clinical manifestations, providing valuable insights into the molecular mechanisms underlying these conditions. Their work has also highlighted the importance of newborn screening for lysosomal storage disorders in Mexico, improving diagnosis and treatment outcomes for affected individuals. These findings have significant implications for personalized medicine and disease prevention.