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Human Molecular Genetics|October 22, 2004
Transcription factor MEF2A mutations in patients with coronary artery diseaseM R Krishna Bhagavatula, Chun Fan, Gong-Qing Shen, et al.Human Molecular Genetics|October 22, 2004
Huntingtin-associated protein 1 (Hap1) mutant mice bypassing the early postnatal lethality are neuroanatomically normal and fertile but display growth retardationIoannis Dragatsis, Scott Zeitlin, Paula DietrichHuman Molecular Genetics|October 22, 2004
Heterologous mitochondrial DNA recombination in human cellsMarilena D'Aurelio, Carl D Gajewski, Michael T Lin, et al.Human Molecular Genetics|June 10, 2005
Mitochondrial localization of the Parkinson's disease related protein DJ-1: implications for pathogenesisLi Zhang, Mika Shimoji, Bobby Thomas, et al.Human Molecular Genetics|June 10, 2005
Foxl2 is required for commitment to ovary differentiationChris Ottolenghi, Shakib Omari, J Elias Garcia-Ortiz, et al.Human Molecular Genetics|May 27, 2005
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndromePetri T Luoma, Ningguang Luo, Wolfgang N Löscher, et al.Human Molecular Genetics|May 13, 2005
Gene expression in Huntington's disease skeletal muscle: a potential biomarkerAndrew D Strand, Aaron K Aragaki, Dennis Shaw, et al.Human Molecular Genetics|May 13, 2005
Distinct pathogenetic mechanisms for PHOX2B associated polyalanine expansions and frameshift mutations in congenital central hypoventilation syndromeTiziana Bachetti, Ivana Matera, Silvia Borghini, et al.Human Molecular Genetics|May 13, 2005
Disruption of Abcc6 in the mouse: novel insight in the pathogenesis of pseudoxanthoma elasticumTheo G M F Gorgels, Xiaofeng Hu, George L Scheffer, et al.Human Molecular Genetics|June 3, 2005
Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistanceDavid A Dyment, Blanca M Herrera, M Zameel Cader, et al.Pageof 1,196