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4. Myopathies due to enzyme deficiencies. Cornelio F; Di Donato S J Neurol; 1985; 232(6):329-40. PubMed ID: 2934518 [TBL] [Abstract][Full Text] [Related]
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8. Laboratory diagnosis of the neuromuscular glycogen storage diseases. Farmer PM Ann Clin Lab Sci; 1982; 12(6):431-8. PubMed ID: 6817693 [TBL] [Abstract][Full Text] [Related]
9. Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases. Burwinkel B; Hu B; Schroers A; Clemens PR; Moses SW; Shin YS; Pongratz D; Vorgerd M; Kilimann MW Eur J Hum Genet; 2003 Jul; 11(7):516-26. PubMed ID: 12825073 [TBL] [Abstract][Full Text] [Related]
11. [Genetic heterogeneity and the diagnosis of hepatic glycogenoses]. Lemonnier A; Baussan C; Moatti N C R Seances Soc Biol Fil; 1984; 178(4):327-47. PubMed ID: 6241011 [TBL] [Abstract][Full Text] [Related]
12. Disorders of glycogen metabolism of muscle. DiMauro S; Bresolin N; Hays AP CRC Crit Rev Clin Neurobiol; 1984; 1(2):83-116. PubMed ID: 6242726 [TBL] [Abstract][Full Text] [Related]
13. Glycogen storage diseases of muscle. DiMauro S; Bruno C Curr Opin Neurol; 1998 Oct; 11(5):477-84. PubMed ID: 9847997 [TBL] [Abstract][Full Text] [Related]