Simon Silver | Jan 7, 1990 | 6 min read
Department of Microbiology & Immunology University of Illinois Chicago - Through cloning and sequence analysis, researchers have identified the primary gene of the hereditary disease muscular dystrophy, thus leading to the characterizing of the primary protein product. Deletions contributing to an absence of the polypeptide dystrophin (0.002% of total muscle protein and 3,685 amino acids long) on the inner surface of the plasma membrane appear to be the primary cause for two types of muscul