By Philip M. Parker
In March 2001, the nationwide Institutes of health and wellbeing issued the next caution: "The variety of websites providing health-related assets grows each day. Many websites offer beneficial info, whereas others could have info that's unreliable or misleading." in addition, a result of speedy elevate in Internet-based details, many hours will be wasted looking, picking out, and printing. given that simply the smallest fraction of knowledge facing 3-methylglutaconic aciduria is listed in se's, resembling www.google.com or others, a non-systematic method of web examine could be not just time eating, but additionally incomplete. This ebook used to be 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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Additional resources for 3-Methylglutaconic Aciduria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
A buildup of somatic mutations in mitochondrial DNA has been associated with some forms of cancer and an increased risk of certain age-related disorders such as heart disease, Alzheimer disease, and Parkinson disease. Additionally, research suggests that the progressive accumulation of these mutations over a person’s lifetime may play a role in the normal process of aging. 40 3-Methylglutaconic Aciduria What Are Complex or Multifactorial Disorders? Researchers are learning that nearly all conditions and diseases have a genetic component.
Cystic fibrosis, sickle cell anemia X-linked dominant X-linked dominant disorders are caused by mutations in genes on the X chromosome. Females are more frequently affected than males, and the chance of passing on an X-linked dominant disorder differs between men and women. Families with an X-linked dominant disorder often have both affected males and affected females in each generation. A striking characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons (no male-to-male transmission).
Source: Pediatric Research. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=1287564&query_hl=16&itool=pubmed_docsum • Mitochondrial complex deficiencies in a male with cardiomyopathy and 3methylglutaconic aciduria. Author(s): Besley GT, Lendon M, Broadhead DM, Till J, Heptinstall LE, Phillips B. Source: Journal of Inherited Metabolic Disease. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=7564252&query_hl=16&itool=pubmed_docsum • Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria.
3-Methylglutaconic Aciduria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker