Track topics on Twitter Track topics that are important to you
Medical researchers have linked the specific biochemical changes to a protein called CHIP to specific disease characteristics of patients with a wide range of rare disorders. The research shows it is possible to merge analyses of protein biochemistry with patient characteristics to better understand spinocerebellar ataxia autosomal recessive 16, or SCAR16.
Original Article: Researchers link specific protein mutations to ataxia disease symptomsNEXT ARTICLE
Within medicine, nutrition (the study of food and the effect of its components on the body) has many different roles. Appropriate nutrition can help prevent certain diseases, or treat others. In critically ill patients, artificial feeding by tubes need t...