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Nature Genetics|May 29, 2002
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemiaRoxanne Y Walder, Daniel Landau, Peter Meyer, et al.Nature Genetics|July 9, 2002
Disruption of dog-1 in Caenorhabditis elegans triggers deletions upstream of guanine-rich DNAIris Cheung, Michael Schertzer, Ann Rose, et al.Nature Genetics|July 23, 2002
Epistatic interaction between KIR3DS1 and HLA-B delays the progression to AIDSMaureen P Martin, Xiaojiang Gao, Jeong-Hee Lee, et al.Nature Genetics|September 1, 1995
Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesisP P Pandolfi, M E Roth, A Karis, et al.Nature Genetics|September 1, 1995
Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6K G Waymire, J D Mahuren, J M Jaje, et al.Nature Genetics|September 1, 1995
Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridizationT Kaneko-Ishino, Y Kuroiwa, N Miyoshi, et al.Nature Genetics|October 1, 1995
Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)J Ahn, H J Lüdecke, S Lindow, et al.Nature Genetics|October 1, 1995
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiencyT Bourgeron, P Rustin, D Chretien, et al.Nature Genetics|October 1, 1995
Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologueS Zeitlin, J P Liu, D L Chapman, et al.Nature Genetics|October 1, 1995
Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolismK Sango, S Yamanaka, A Hoffmann, et al.Pageof 744