Alexander Disease - A Bibliography and Dictionary for by Philip M. Parker PDF

By Philip M. Parker

ISBN-10: 0497113201

ISBN-13: 9780497113209

ISBN-10: 1429496177

ISBN-13: 9781429496179

In March 2001, the nationwide Institutes of well-being issued the next caution: "The variety of websites providing health-related assets grows on a daily basis. Many websites supply worthwhile info, whereas others could have info that's unreliable or misleading." additionally, due to the speedy elevate in Internet-based details, many hours might be wasted looking, determining, and printing. considering that purely the smallest fraction of data facing Alexander affliction is listed in se's, akin to www.google.com or others, a non-systematic method of web study should be not just time eating, but in addition incomplete. This booklet used to be created for doctors, scholars, and contributors of most people who are looking to behavior scientific study utilizing the main complicated instruments to be had and spending the smallest amount of time doing so.

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Extra resources for Alexander Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

Sample text

DNA segments with an abnormal number of these repeats are unstable and prone to errors during cell division. The number of repeats can change as the gene is passed from parent to child. If the number of repeats increases, it is known as a trinucleotide repeat expansion. In some cases, the trinucleotide repeat may expand until the gene stops functioning normally. This expansion causes the features of some disorders to become more severe with each successive generation. Most genetic disorders have signs and symptoms that differ among affected individuals, including affected people in the same family.

Acquired (or somatic) mutations occur in the DNA of individual cells at some time during a person’s life. These changes can be caused by environmental factors such as ultraviolet radiation from the sun, or can occur if a mistake is made as DNA copies itself during cell division. Acquired mutations in somatic cells (cells other than sperm and egg cells) cannot be passed on to the next generation. Mutations may also occur in a single cell within an early embryo. As all the cells divide during growth and development, the individual will have some cells with the mutation and some cells without the genetic change.

Mutations that occur only in an egg or sperm cell, or those that occur just after fertilization, are called new (de novo) mutations. De novo mutations may explain genetic disorders in which an affected child has a mutation in every cell, but has no family history of the disorder. Acquired (or somatic) mutations occur in the DNA of individual cells at some time during a person’s life. These changes can be caused by environmental factors such as ultraviolet radiation from the sun, or can occur if a mistake is made as DNA copies itself during cell division.

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Alexander Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker


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