Increased urine concentration of subunit c of mitochondrial ATP synthase in neuronal ceroid lipofuscinoses patients
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF00711619
Reference13 articles.
1. Armstrong D, Wehling C, Wormer DV (1977) Diagnosis of Batten disease from urinary sediment.Pathology 9: 39?41.
2. Bennett MJ, Mathers NJ, Hemming FW, Zweije-Hofman I, Hosking GP (1985) Urinary sediment dolichol excretion in patients with Batten disease and other neurodegenerative and storage disorders.Pediatr Res 19: 213?216.
3. de Baecque C (1975) Diagnosis of neuronal ceroid lipofuscinosis by electron microscopy of urinary sediment.N Engl J Med 292: 1408.
4. Dolman CL, McLeod PM, Chang EC (1980) Lymphocytes and urine in ceroid lipofuscinosis.Arch Pathol Lab Med 104: 487?490.
5. Fearnley IM, Walker JE, Martinus RD et al (1990) The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarboimid-reactive proteolipid of mitochondrial ATP synthase.Biochem J 268: 751?758.
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