Co-cultivation of Niemann-Pick disease type C fibroblasts belonging to complementation groupsα andβ stimulates LDL-derived cholesterol esterification
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799171
Reference8 articles.
1. Blanchette-Mackie EJ, Dwyer NK, Vanier MT, et al (1989) Type C Niemann-Pick disease: dimethyl sulfoxide moderates abnormal LDL-cholesterol processing in mutant fibroblasts.Biochim Biophys Acta 1006: 219–226.
2. Carstea ED, Polymeropoulos MH, Parker CC, et al (1993) Linkage of Niemann-Pick disease type C to human chromosome 18.Proc Natl Acad Sci USA 90: 2002–2004.
3. Neville BGR, Lake BD, Stephens R, Sanders MD (1973) A neurovisceral storage disease with vertical supranuclear ophthalmoplegia and its relationships to Niemann-Pick disease.Brain 96: 97–120.
4. Steinberg SJ, Ward CP, Fensom AH (1994) Complementation studies in Niemann-Pick disease type C indicate the existence of a second group.J Med Genet 31: 317–320.
5. Vanier MT, Pentchev P, Rodriguez-Lafrasse C, Rousson R (1991a) Niemann-Pick disease type C: an update.J Inher Metab Dis 14: 580–595.
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