Is central core disease with structural core a fetal defect?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
http://link.springer.com/content/pdf/10.1007/BF00313941.pdf
Reference28 articles.
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3. Baril EF, Love DS, Herrmann H (1966) Investigation of myosin heterogenity observed during chromatography on diethyl-aminoethyl cellulose. J Biol Chem 241:822–830
4. Bethlem J, Cool J van, Hulsmann WC, Meijer AEFH (1966) Familial non-progressive myopathy with muscle cramps after exercise. A new disease associated with cores in the muscle fibres. Brain 89:569–588
5. Cohen ME, Duffner PK, Heffner R (1978) Central core disease in one of identical twins. J Neurol Neurosurg Psychiatry 41:659–663
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1. Congenital (Structural) Myopathies;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
2. Main steps of skeletal muscle development in the human;Handbook of Clinical Neurology;2013
3. Central core disease: Ultrastructure of the sarcoplasmic reticulum and T-tubules;Muscle & Nerve;1989-02
4. Orthopaedic aspects of central core disease.;The Journal of Bone & Joint Surgery;1988-08
5. Central Core Disease;Medicine;1987-09
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