Nondystrophic Myotonia
What's New
Last Posted: Feb 17, 2023
- Sequence CLCN1 and SCN4A genes in patients with nondystrophic myotonia in Chinese people.
Meng Yan-Xin, et al. Medicine 2022 0 (29) e29591 - Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenita.
Modoni Anna, et al. Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society 2011 0 (1) 39-44 - Nondystrophic myotonia
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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