Baumann P., Myllyla VV, Leisti J.: Myotonia congenita in northern Finland: An epidemiological and genetic study . J Med Genet35: 293-296, 1998
2.
Becker PE: Myotonia Congenita & Symptoms Associated with Myotonia. Stuttgart, Georg Thieme Publishers, 1977
3.
George ALJr ,Sloan-Brown K., Fenichel GM, et al: Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita. Hum Mol Genet3: 2071-2072, 1994
4.
Hoffman EP, Lehmann-Horn F., Rüdel R.: Overexcited or inactive: Ion channels in muscle disease. Cell80: 681-686, 1995
5.
Koch MC, Steinmeyer K., Lorenz C., et al: The skeletal muscle chloride channel in dominant and recessive human myotonia. Science257: 797- 800, 1992
6.
Kurtzke JF, Kurkland LT: The epidemiology of neurologic disease, in Joynt RJ (ed): Clinical Neurology. Volume 4. Philadelphia, JB Lippincott Co , 1993, pp 1-143
7.
Kwiecinski H. , Ryniewicz B., Ostrzycki A.: Treatment of myotonia with antiarrhythmic drugs. Acta Neurol Scand86: 371-375, 1992
8.
McManis PG, Lambert EH, Daube JR: The exercise test in periodic paralysis. Muscle Nerve9: 704-710, 1986
9.
Pinessi L., Bergamini L., Cantello R., et al: Myotonia congenita and myotonic dystrophy: Descriptive epidemiological investigation in Turin, Italy (1955-1979). Ital J Neurol Sci3: 207-210, 1982
10.
Ptacek LJ, Johnson KJ, Griggs RC: Genetics and physiology of the myotonic muscle disorders. N Engl J Med328: 482-489, 1993
11.
Rudel R., Lehmann-Horn F., Ricker K.: The nondystrophic myotonias, in Engel AG, Franzini-Armstrong C (eds): Myology. Second edition. Volume 2. New York, McGraw-Hill, 1994, pp 1291-1300
12.
Thomsen J.: Tonische Krämpfe in willkürlich beweglichen Muskeln in Folge von erebter psychischer Disposition. Arch Psychiatr Nervenkr6: 702, 1876