HuGE Literature Finder
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Records 1-3
Sample-to-SNP kit: a reliable, easy and fast tool for the detection of HFE p.H63D and p.C282Y variations associated to hereditary hemochromatosis.
Gene 2012 Oct 507 (1): 79-84. Nielsen Peter B, Petersen Maja S, Ystaas Viviana, Andersen Rolf V, Hansen Karin M, Blaabjerg Vibeke, Refstrup Met |
Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia.
Journal of neurology 2012 Feb 259 (2): 246-50. Sánchez-Ferrero Elena, Coto Eliecer, Corao Ana I, Díaz Marta, Gámez Josep, Esteban Jesús, Gonzalo Juan F, Pascual-Pascual Samuel I, López De Munaín Adolfo, Morís Germán, Infante Jon, Del Castillo Emilia, Márquez Celedonio, Alvarez Victor |
Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
Journal of human genetics 2010 Mar 55 (3): 147-54. Kato Tomofumi, Nishigaki Yutaka, Noguchi Yoshihiro, Ueno Hitomi, Hosoya Hiroko, Ito Taku, Kimura Yurika, Kitamura Ken, Tanaka Masas |
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- Page last updated:Dec 5, 2019
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