Corrigendum: PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron
暂无分享,去创建一个
Colin A. Johnson | N. Nardocci | R. Trembath | B. Levinson | J. Gitschier | N. Canham | J. Morton | D. Rodriguez | B. Wilmot | S. Westaway | I. Desguerre | P. Kramer | J. Coryell | P. Gissen | E. Maher | A. Simonati | G. Zorzi | C. Woods | N. Morgan | E. Bertini | A. Gregory | S. Hayflick | C. Schanen | H. Cangul | S. Pasha | Scott Sonek | A. Mubaidin
[1] Colin A. Johnson,et al. PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron , 2006, Nature Genetics.
[2] D. Watkins,et al. Complementation studies in the cblAclass of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH) , 2000, Journal of medical genetics.
[3] E. Shoubridge,et al. Expression and functional analysis of SURF1 in Leigh syndrome patients with cytochrome c oxidase deficiency. , 1999, Human molecular genetics.
[4] D. Watkins. Cobalamin metabolism in methionine-dependent human tumour and leukemia cell lines. , 1998, Clinical and investigative medicine. Medecine clinique et experimentale.
[5] P. Green,et al. Consed: a graphical tool for sequence finishing. , 1998, Genome research.
[6] P. Green,et al. Base-calling of automated sequencer traces using phred. I. Accuracy assessment. , 1998, Genome research.
[7] A. Miller,et al. Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production , 1986, Molecular and cellular biology.