Storage bodies in the ceroid-lipofuscinoses (Batten disease): Low-molecular-weight components, unusual amino acids and reconstitution of fluorescent bodies from non-fluorescent components
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF00710268
Reference11 articles.
1. Fearnley IM, Walker JE, Martinus RD, Jolly RD et al (1990). The sequence of the major protein stored in ovine ceroid-lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase.Biochem J 268: 751?758.
2. Jolly RD, Martinus RD, Palmer DN (1992) Sheep and other animals with ceroid-lipofuscinoses: Their relevance to Batten disease.Am J Med Genet 42: 609?614.
3. Katz ML, Gerhardt KO (1990) Storage protein in hereditary ceroid-lipofuscinosis containsS-methylated methionine.Mech Ageing Dev 53: 277?290.
4. Katz ML, Gerhardt KO (1992) Methylated lysine in storage body protein of sheep with hereditary ceroid-lipofuscinosis.Biochim Biophys Acta 1138: 97?108.
5. Katz ML, Rodrigues M (1991) Juvenile ceroid lipofuscinosis. Evidence for methylated lysine in neural storage body protein.Am J Pathol 138: 323?332.
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