Using intense X-rays from the Stanford Synchrotron Radiation Lightsource, researchers have determined the detailed structure of a key part of the ryanodine receptor, a protein associated with calcium-related disease. Their results, which combine data from SSRL and the Canadian Light Source, pinpoint the locations of more than 50 mutations that cluster in disease "hotspots" along the receptor and offer insights into how the mutations might cause the receptor to malfunction.