Recent advances in the molecular genetics of the neuronal ceroid lipofuscinoses
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799253
Reference30 articles.
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3. Ezaki J, Wolfe LS, Ishidoh K, Kominami E (1995) Abnormal degradative pathway of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid-lipofuscinosis (Batten disease).Am J Med Genet 47: 254–259.
4. Faisal Khan KM, Sklower Brooks S, Pullarkat RK (1995) Abnormal acid phosphatases in neuronal ceroid-lipofuscinoses.Am J Med Genet 57: 285–289.
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 dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase.Biochem J 268: 751–758.
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4. The neuronal ceroid-lipofuscinoses (Batten disease): A new class of lysosomal storage diseases;Journal of Inherited Metabolic Disease;1999-06
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