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Nature Genetics|February 1, 1997
Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutationL Mangiarini, K Sathasivam, A Mahal, et al.Nature Genetics|February 1, 1997
Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acidsR W Taylor, P F Chinnery, D M Turnbull, et al.Nature Genetics|November 1, 1996
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2S M Pulst, A Nechiporuk, T Nechiporuk, et al.Nature Genetics|November 1, 1996
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECTK Sanpei, H Takano, S Igarashi, et al.Nature Genetics|November 1, 1996
The effect of the human serum paraoxonase polymorphism is reversed with diazoxon, soman and sarinH G Davies, R J Richter, M Keifer, et al.Nature Genetics|November 1, 1996
Mutations in the testis/liver isoform of the phosphorylase kinase gamma subunit (PHKG2) cause autosomal liver glycogenosis in the gsd rat and in humansA J Maichele, B Burwinkel, I Maire, et al.Nature Genetics|February 1, 1993
Genetic mosaicism in normal tissues of Wilms' tumour patientsL Y Chao, V Huff, G Tomlinson, et al.Nature Genetics|October 1, 1996
Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNAJ P Jenuth, A C Peterson, K Fu, et al.Nature Genetics|October 1, 1996
The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4- phosphate 5-kinaseJ J Carvajal, M A Pook, M dos Santos, et al.Nature Genetics|October 1, 1996
A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindnessH Jin, M May, L Tranebjaerg, et al.Pageof 744