By Philip M. Parker
In March 2001, the nationwide Institutes of well-being issued the next caution: "The variety of sites delivering health-related assets grows on a daily basis. Many websites offer helpful info, whereas others can have info that's unreliable or misleading." in addition, due to the swift raise in Internet-based info, many hours could be wasted looking, choosing, and printing. due to the fact purely the smallest fraction of data facing 3-methylglutaconic aciduria is listed in se's, reminiscent of www.google.com or others, a non-systematic method of web study might be not just time eating, but in addition incomplete. This ebook was once created for doctors, scholars, and contributors of most of the people who are looking to behavior scientific study utilizing the main complex instruments to be had and spending the smallest amount of time doing so.
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Additional resources for 3-Methylglutaconic Aciduria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
Source: Journal of Pediatric Hematology/Oncology : Official Journal of the American Society of Pediatric Hematology/Oncology. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=16462576&query_hl=16&itool=pubmed_docsum • Nephrocalcinosis and medullary cysts in 3-methylglutaconic aciduria. Author(s): Laube GF, Leonard JV, van't Hoff WG. Source: Pediatric Nephrology (Berlin, Germany). db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=12750979&query_hl=16&itool=pubmed_docsum • NMR spectroscopic studies on the late onset form of 3-methylglutaconic aciduria type I and other defects in leucine metabolism.
Autosomal dominant disorders tend to occur in every generation of an affected family. Examples Huntington disease, neurofibromatosis type 1 Help Me Understand Genetics 45 Autosomal recessive Two mutated copies of the gene are present in each cell when a person has an autosomal recessive disorder. An affected person usually has unaffected parents who each carry a single copy of the mutated gene (and are referred to as carriers). Autosomal recessive disorders are typically not seen in every generation of an affected family.
These types of RNA help assemble protein building blocks (amino acids) into functioning proteins. What Is a Gene? A gene is the basic physical and functional unit of heredity. Genes, which are made up of DNA, act as instructions to make molecules called proteins. In humans, genes vary in size from a few hundred DNA bases to more than 2 million bases. The Human Genome Project has estimated that humans have between 20,000 and 25,000 genes. Every person has two copies of each gene, one inherited from each parent.
3-Methylglutaconic Aciduria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker
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