By Philip M. Parker

In March 2001, the nationwide Institutes of overall healthiness issued the subsequent caution: "The variety of sites supplying health-related assets grows on a daily basis. Many websites supply necessary info, whereas others could have info that's unreliable or misleading." additionally, as a result of quick raise in Internet-based details, many hours may be wasted looking out, deciding upon, and printing. in view that simply the smallest fraction of knowledge facing 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency is listed in se's, comparable to www.google.com or others, a non-systematic method of net examine could be not just time eating, but additionally incomplete. This ebook was once created for doctors, scholars, and contributors of most of the people who are looking to behavior clinical examine utilizing the main complex instruments to be had and spending the smallest amount of time doing so.

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Extra info for 3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

Example text

The DNA sequence of a gene can be altered in a number of ways. Gene mutations have varying effects on health, depending on where they occur and whether they alter the function of essential proteins. The types of mutations include: • Missense mutation: This type of mutation is a change in one DNA base pair that results in the substitution of one amino acid for another in the protein made by a gene. • Nonsense mutation: A nonsense mutation is also a change in one DNA base pair. Instead of substituting one amino acid for another, however, the altered DNA sequence prematurely signals the cell to stop building a protein.

Changes that affect entire chromosomes or segments of chromosomes can cause problems with growth, development, and function of the body’s systems. These changes can affect many genes along the chromosome and alter the proteins made by those genes. Conditions caused by a change in the number or structure of chromosomes are known as chromosomal disorders. Human cells normally contain 23 pairs of chromosomes, for a total of 46 chromosomes in each cell. A change in the number of chromosomes leads to a chromosomal disorder.

Human cells normally contain 23 pairs of chromosomes, for a total of 46 chromosomes in each cell. A change in the number of chromosomes leads to a chromosomal disorder. These 30 3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency changes can occur during the formation of reproductive cells (eggs and sperm) or in early fetal development. A gain or loss of chromosomes from the normal 46 is called aneuploidy. The most common form of aneuploidy is trisomy, or the presence of an extra chromosome in each cell.

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