Duchenne muscular dystrophy and idiopathic hyperCKemia in the same family

Author:

Eeg-Olofsson Orvar,Kalimo Hannu,Eeg-Olofsson Karin Edebol,Jagell Sten,Marklund Lena,Simonsson Linda,Dahl Niklas

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference9 articles.

1. Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair;Stallings;Am J Hum Genet,1988

2. HyperCKemia and rhabdomyolysis;Svoboda,2003

3. Familial idiopathic hyper-CK-emia: an underrecognized condition;Capasso;Muscle Nerve,2006

4. Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family;Frydman;Am J Med Genet,1995

5. Duchenne muscular dystrophy and idiopathic hyperCkemia in a family causing confusion in genetic counselling;Bushby;Am J Med Genet,1996

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Asymptomatic HyperCKemia;Managing Myositis;2019-12-15

2. Significance of Asymptomatic Hyper Creatine-Kinase Emia;Journal of Clinical Neuromuscular Disease;2019-12

3. Approach to asymptomatic creatine kinase elevation;Cleveland Clinic Journal of Medicine;2016-01

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