By Philip M. Parker
ISBN-10: 0497112493
ISBN-13: 9780497112493
In March 2001, the nationwide Institutes of wellbeing and fitness issued the subsequent caution: "The variety of sites delivering health-related assets grows each day. Many websites supply worthwhile info, whereas others can have details that's unreliable or misleading." moreover, as a result swift elevate in Internet-based info, many hours may be wasted looking, settling on, and printing. on account that basically the smallest fraction of knowledge facing Leber hereditary optic neuropathy is listed in se's, corresponding to www.google.com or others, a non-systematic method of net study might be not just time eating, but additionally incomplete. This publication used to be created for doctors, scholars, and participants 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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Additional resources for Leber Hereditary Optic Neuropathy - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
Example text
Author(s): Howell N, Mackey DA. Source: American Journal of Human Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=9867707&query_hl=50&itool=pubmed_docsum • Microphotometric analysis of NADH-tetrazolium reductase deficiency in fibroblasts of patients with Leber hereditary optic neuropathy. Author(s): Malik S, Sudoyo H, Marzuki S. Source: Journal of Inherited Metabolic Disease. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=11117434&query_hl=50&itool=pubmed_docsum • Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation.
Author(s): Mackey DA, Oostra RJ, Rosenberg T, Nikoskelainen E, Bronte-Stewart J, Poulton J, Harding AE, Govan G, Bolhuis PA, Norby S. Source: American Journal of Human Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=8755941&query_hl=50&itool=pubmed_docsum • Progression of visual field defects in Leber hereditary optic neuropathy: experience of the LHON treatment trial. Author(s): Newman NJ, Biousse V, Newman SA, Bhatti MT, Hamilton SR, Farris BK, Lesser RL, Turbin RE. Source: American Journal of Ophthalmology.
Source: Proceedings of the National Academy of Sciences of the United States of America. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=8016139&query_hl=50&itool=pubmed_docsum • A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I. Author(s): Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, Wallace DC. Source: American Journal of Human Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=1322638&query_hl=50&itool=pubmed_docsum Studies 27 • A new sequence variant in mitochondrial DNA associated with high penetrance of Russian Leber hereditary optic neuropathy.
Leber Hereditary Optic Neuropathy - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker
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