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Nature Genetics|November 4, 2000
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23A G Gharavi, Y Yan, F Scolari, et al.Nature Genetics|September 6, 2000
Mutations in MKKS cause Bardet-Biedl syndromeA M Slavotinek, E M Stone, K Mykytyn, et al.Nature Genetics|September 6, 2000
Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complexL S Kirschner, J A Carney, S D Pack, et al.Nature Genetics|September 6, 2000
Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomalyM J Kelley, W Jawien, T L Ortel, et al.Nature Genetics|September 6, 2000
Nf1;Trp53 mutant mice develop glioblastoma with evidence of strain-specific effectsK M Reilly, D A Loisel, R T Bronson, et al.Nature Genetics|September 6, 2000
Identification of the gene causing mucolipidosis type IVR Bargal, N Avidan, E Ben-Asher, et al.Nature Genetics|January 4, 2001
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3C L Bennett, J Christie, F Ramsdell, et al.Nature Genetics|January 4, 2001
A biochemical function for attractin in agouti-induced pigmentation and obesityL He, T M Gunn, D M Bouley, et al.Nature Genetics|January 4, 2001
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessH S Scott, J Kudoh, M Wattenhofer, et al.Nature Genetics|January 4, 2001
Bone morphogenetic protein-3 is a negative regulator of bone densityA Daluiski, T Engstrand, M E Bahamonde, et al.Pageof 745