By Philip M. Parker
ISBN-10: 0497112914
ISBN-13: 9780497112912
ISBN-10: 1429496460
ISBN-13: 9781429496469
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Extra info for Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
Sample text
Proteins are made up of hundreds or thousands of smaller units called amino acids, which are attached to one another in long chains. There are 20 different types of amino acids that can be combined to make a protein. The sequence of amino acids determines each protein’s unique 3-dimensional structure and its specific function. 22 Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency Examples of Protein Functions Proteins can be described according to their large range of functions in the body, listed in alphabetical order: Function Antibody Description Antibodies bind to specific foreign particles, such as viruses and bacteria, to help protect the body.
Disorders with mitochondrial inheritance result from mutations in mitochondrial DNA. Although mitochondrial 36 Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency disorders can affect both males and females, only females can pass mutations in mitochondrial DNA to their children. A woman with a disorder caused by changes in mitochondrial DNA will pass the mutation to all of her daughters and sons, but the children of a man with such a disorder will not inherit the mutation. It is important to note that the chance of passing on a genetic condition applies equally to each pregnancy.
This term includes both newly diagnosed and preexisting cases in people of any age. Prevalence is often written in the form “1 in [a number]” or as a total number of people who have a condition. Approximately 1 in 100,000 people in the United States have syndrome A at the present time. About 100,000 children worldwide currently have syndrome B. Mortality Mortality is the number of deaths from a particular disorder occurring in a specified group per year. Mortality is usually expressed as a total number of deaths.
Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker
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