Author:
Bakker H. D.,Taminiau J. A. J. M.,van den Berg J. E. T.,Berger R.
Subject
Genetics(clinical),Genetics
Reference3 articles.
1. Huijing, F. and Fernandes, J. X-Chromosomal inheritance of liver glycogenosis with phosphorylase kinase deficiency.Am. J. Hum. Genet. 21 (1969) 275–284
2. Lederer, B., van Hoof, F., van den Berghe, G. and Hers, H.G. Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen storage disease. A study of phosphorylase kinase deficiency.Biochem. J. 147 (1975) 23–35
3. Ohtani, Y., Matsuda, J., Iwamasa, T., Tamari, H., Origuchi, Y. and Miike, T. Infantile glycogen storage myopathy in a girl with phosphorylase kinase deficiency.Neurology 32 (1982) 833–838
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