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Results 1 - 10 of 14 for Amyotrophic lateral sclerosis type 10
  1. Amyotrophic lateral sclerosis 
    ... in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science. 2009 Feb 27;323(5918):1208-1211. doi: 10.1126/science.1165942. Citation on PubMed or Free ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  2. FUS gene 
    ... in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science. 2009 Feb 27;323(5918):1208-1211. doi: 10.1126/science.1165942. Citation on PubMed or Free ...
    https://medlineplus.gov/genetics/gene/fus - Genetics
  3. C19orf12 gene 
    ... to have a condition called hereditary spastic paraplegia type 43. More About This Health Condition ... iron accumulation mimicking juvenile amyotrophic lateral sclerosis. J Neurol. 2012 Nov;259(11):2434-9. doi: 10.1007/s00415-012-6521-7. Epub 2012 May ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics
  4. Distal myopathy 2 
    ... pharyngeal weakness with distal myopathy Genetic Testing Registry: Amyotrophic lateral sclerosis type 21 Vocal cord and pharyngeal distal myopathy National ...
    https://medlineplus.gov/genetics/condition/distal-myopathy-2 - Genetics
  5. SOD1 gene 
    ... Zittin Potter S. Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis. Annu Rev Biochem. 2005;74:563-93. doi: 10.1146/annurev.biochem.72.121801.161647. Citation on ...
    https://medlineplus.gov/genetics/gene/sod1 - Genetics
  6. SETX gene 
    ... PJ. Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis. Nat Rev Neurol. 2011 Nov;7(11):616-30. doi: 10.1038/nrneurol.2011.152. Citation on PubMed Fogel ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  7. C9orf72 gene 
    ... the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. Lancet Neurol. 2012 Apr;11(4):323-30. doi: 10.1016/S1474-4422(12)70043-1. Epub 2012 ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  8. Charcot-Marie-Tooth disease 
    ... the nerve impulse. People with CMT2 may develop amyotrophic lateral sclerosis ... as intermediate type, the nerve impulses are both slowed and reduced ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  9. SPG11 gene 
    ... cause the signs and symptoms of spastic paraplegia type 11 by interfering with the protein's ... This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  10. ATXN2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition ... Lastres-Becker I, Rub U, Auburger G. Spinocerebellar ataxia 2 (SCA2). Cerebellum. 2008;7(2):115-24. doi: 10.1007/s12311-008-0019-y. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/atxn2 - Genetics
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