Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and POLG2[original query] |
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| Identification of two gene variants associated with risk of advanced fibrosis in patients with chronic hepatitis C. Gastroenterology 2006 May 130 (6): 1679-87. Huang Hongjin, Shiffman Mitchell L, Cheung Ramsey C, Layden Thomas J, Friedman Scott, Abar Olivia T, Yee Linda, Chokkalingam Anand P, Schrodi Steven J, Chan Jason, Catanese Joseph J, Leong Diane U, Ross David, Hu Xiaolan, Monto Alexander, McAllister Linda B, Broder Samuel, White Thomas, Sninsky John J, Wright Teresa |
| What is influencing the phenotype of the common homozygous polymerase-? mutation p.Ala467Thr? Brain : a journal of neurology 2012 Dec 135 (Pt 12): Pt 12. Neeve VC, Samuels DC, Bindoff LA, van den Bosch B, Van Goethem G, Smeets H, Lombès A, Jardel C, Hirano M, Dimauro S, De Vries M, Smeitink J, Smits BW, de Coo IF, Saft C, Klopstock T, Keiling BC, Czermin B, Abicht A, Lochmüller H, Hudson G, Gorman GG, Turnbull DM, Taylor RW, Holinski-Feder E, Chinnery PF, Horvath R |
Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study.
Frontiers in genetics 2013 4 310. Lee Joseph H, Cheng Rong, Honig Lawrence S, Feitosa Mary, Kammerer Candace M, Kang Min S, Schupf Nicole, Lin Shiow J, Sanders Jason L, Bae Harold, Druley Todd, Perls Thomas, Christensen Kaare, Province Michael, Mayeux Richa |
| Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging. Mitochondrion 2015 Dec 26 81-85. Paramasivam Arumugam, Meena Angamuthu Kannan, Pedaparthi Lalitha, Jyothi Vuskamalla, Uppin Megha S, Jabeen Shaikh Afshan, Sundaram Challa, Thangaraj Kumarasa |
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