Author:
Mori Masayuki,Nishimura Masahiko
Publisher
Springer Science and Business Media LLC
Reference36 articles.
1. Boison D, Stoffel W (1989) Myelin-deficient rat: a point mutation in exon III (A → C, Thr75 → Pro) of the myelin proteolipid protein causes dysmyelination and oligodendrocyte death. EMBO J 8, 3295–3302
2. Camakaris J, Danks DM, Ackland L, Cartright E, Borger P, Cotton RGH (1980) Altered copper metabolism in cultured cells from human Menkes’ syndrome and mottled mouse mutants. Biochem Genet 18, 117–131
3. Cecchi C, Avner P (1996) Genomic organization of the mottled gene, the mouse homologue of the human Menkes disease gene. Genomics 37, 96–104
4. Chelly J, Turner Z, Tonnesen T, Petterson A, Ishikawa-Brush Y, Tommerup N, Horn N, Monaco AP (1993) Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein. Nature Genet 3, 14–19
5. Das S, Levinson B, Whitney S, Vulpe C, Packman S (1994) Diverse mutations in patients with Menkes disease often lead to exon skipping. Am J Hum Genet 55, 883–889
Cited by
25 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献