Diagnosis of a novel glycogen storage disease: Type 1aSP
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799362
Reference8 articles.
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2. Burchell, A., Jung, R. T., Lang, C. C., Bennet, W. and Shepherd, A. N. Diagnosis of type 1a and type 1c glycogen storage diseases in adults.Lancet 1 (1987) 1059–1062
3. Burchell, A., Hume, R. and Burchell, B. A new microtechnique for the analysis of the human hepatic microsomal glucose-6-phosphatase system.Clin. Chim. Acta. 173 (1988a) 183–192
4. Burchell, A., Waddell, I. D., Countaway, J. L., Arion, W. J. and Hume, R. Identification of the human hepatic microsomal glucose-6-phosphatase enzyme.FEBS Lett. 242 (1988b) 153–156
5. Countaway, J. L., Waddell, I. D., Burchell, A. and Arion, W. J. The phosphohydrolase component of the hepatic microsomal glucose-6-phosphatase system is a 36.5-kilodalton polypeptide.J. Biol. Chem. 263 (1988) 2673–2678
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