By Philip M. Parker
In March 2001, the nationwide Institutes of health and wellbeing issued the subsequent caution: "The variety of sites providing health-related assets grows each day. Many websites supply worthy details, whereas others could have info that's unreliable or misleading." moreover, as a result of the speedy raise in Internet-based info, many hours should be wasted looking out, identifying, and printing. given that basically the smallest fraction of knowledge facing Carnitine palmitoyltransferase II deficiency is listed in se's, corresponding to www.google.com or others, a non-systematic method of net learn may be not just time eating, but in addition incomplete. This booklet was once created for doctors, scholars, and individuals of most people who are looking to behavior clinical 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 Carnitine Palmitoyltransferase II Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
They are common enough to be considered a normal variation in the DNA. gov/handbook. 32 Carnitine Palmitoyltransferase II Deficiency responsible for many of the normal differences between people such as eye color, hair color, and blood type. Although many polymorphisms have no negative effects on a person’s health, some of these variations may influence the risk of developing certain disorders. How Can Gene Mutations Affect Health and Development? To function correctly, each cell depends on thousands of proteins to do their jobs in the right places at the right times.
Different researchers investigating the same gene may each give the gene a different name, which can cause confusion. The HGNC assigns a unique name and symbol to each human gene, which allows effective organization of genes in large databanks, aiding the advancement of research. For specific information about how genes are named, refer to the HGNC’s Guidelines for Human Gene Nomenclature. Genetics Home Reference describes genes using the HGNC’s official gene names and gene symbols. Genetics Home Reference frequently presents the symbol and name separated with a colon (for example, FGFR4: Fibroblast growth factor receptor 4).
It is important to note that genes themselves do not cause disease—genetic disorders are caused by mutations that make a gene function improperly. For example, when people say that someone has “the cystic fibrosis gene,” they are usually referring to a mutated version of the CFTR gene, which causes the disease. All people, including those without cystic fibrosis, have a version of the CFTR gene. Do All Gene Mutations Affect Health and Development? No, only a small percentage of mutations cause genetic disorders—most have no impact on health or development.
Carnitine Palmitoyltransferase II Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker