Download PDF by Philip M. Parker: 3-Methylglutaconic Aciduria - A Bibliography and Dictionary

By Philip M. Parker

ISBN-10: 0497112000

ISBN-13: 9780497112004

ISBN-10: 1429497343

ISBN-13: 9781429497343

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In March 2001, the nationwide Institutes of well-being issued the subsequent caution: "The variety of sites supplying health-related assets grows each day. Many websites supply worthwhile details, whereas others could have info that's unreliable or deceptive. " additionally, as a result of fast bring up in Internet-based info, many hours could be wasted looking, settling on, and printing.

Additional resources for 3-Methylglutaconic Aciduria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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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.

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3-Methylglutaconic Aciduria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker


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