Subject
Genetics (clinical),Genetics
Reference12 articles.
1. Corzo D, Gibson W, Johnson K, et al (2002) Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders. Am J Hum Genet 70: 1520–1531.
2. Ferdinandusse S, Kostopoulos P, Denis S, et al (2006) Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathy. Am J Hum Genet 78: 1046–1052.
3. Moser HW, Smith KD, Watkins PA, Powers J, Moser AB (2001) X-linked adrenoleukodystrophy. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds; Childs B, Kinzler KW, Vogelstein B, assoc, eds. The Metabolic and Molecular Bases of Inherited Disease, 8th edn. New York: McGraw-Hill, 3257–3301.
4. Shimozawa N, Tsukamoto T, Suzuki Y, et al (1992) A human gene responsible for Zellweger syndrome that affects peroxisome assembly. Science 255: 1132–1134.
5. Shimozawa N, Suzuki Y, Zhang Z, et al (1998) Genetic basis of peroxisome assembly mutants of humans, CHO cells and yeast: identification of a new complementation group of peroxisome biogenesis disorders, absent from peroxisomal membrane ghosts. Am J Hum Genet 63: 1898–1903.
Cited by
38 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