Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase.
Gospe, S M
Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase. [electronic resource] - Neurology Oct 1998 - 1228-9 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0028-3878
10.1212/wnl.51.4.1228 doi
Adolescent
Creatine Kinase--blood
Female
Glycogen Storage Disease Type V--genetics
Humans
Muscle, Skeletal--enzymology
Mutation
Phosphorylases--blood
Polymorphism, Restriction Fragment Length
Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase. [electronic resource] - Neurology Oct 1998 - 1228-9 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0028-3878
10.1212/wnl.51.4.1228 doi
Adolescent
Creatine Kinase--blood
Female
Glycogen Storage Disease Type V--genetics
Humans
Muscle, Skeletal--enzymology
Mutation
Phosphorylases--blood
Polymorphism, Restriction Fragment Length