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Nature Genetics|August 3, 2004
Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19Heng F Seow, Stefan Bröer, Angelika Bröer, et al.Nature Genetics|August 10, 2004
Mutations in a new member of the chromodomain gene family cause CHARGE syndromeLisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, et al.Nature Genetics|December 14, 2004
Modular epistasis in yeast metabolismDaniel Segrè, Alexander Deluna, George M Church, et al.Nature Genetics|December 14, 2004
Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type IbMurat Bastepe, Leopold F Fröhlich, Agnès Linglart, et al.Nature Genetics|February 26, 2005
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth diseaseStephan Züchner, Maher Noureddine, Marina Kennerson, et al.Nature Genetics|February 26, 2005
Pyrexia is a new thermal transient receptor potential channel endowing tolerance to high temperatures in Drosophila melanogasterYoungseok Lee, Yong Lee, Jaejung Lee, et al.Nature Genetics|March 1, 2005
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing lossJost Schönberger, Libin Wang, Jordan T Shin, et al.Nature Genetics|March 8, 2005
Frequent somatic mutations of the transcription factor ATBF1 in human prostate cancerXiaodong Sun, Henry F Frierson, Ceshi Chen, et al.Nature Genetics|February 22, 2005
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulinEdgar A Otto, Bart Loeys, Hemant Khanna, et al.Nature Genetics|January 28, 2004
Regulation of flowering time by FVE, a retinoblastoma-associated proteinIsrael Ausín, Carlos Alonso-Blanco, José A Jarillo, et al.Pageof 745