TY  - GEN
AU  - Gospe,S M
AU  - El-Schahawi,M
AU  - Shanske,S
AU  - Bruno,C
AU  - DiMauro,S
AU  - Hoye,E
AU  - Walsh,D A
AU  - Gorin,F A
TI  - Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase
SN  - 0028-3878
PY  - 1998///1030
KW  - Adolescent
KW  - Creatine Kinase
KW  - blood
KW  - Female
KW  - Glycogen Storage Disease Type V
KW  - genetics
KW  - Humans
KW  - Muscle, Skeletal
KW  - enzymology
KW  - Mutation
KW  - Phosphorylases
KW  - Polymorphism, Restriction Fragment Length
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/wnl.51.4.1228
ER  -