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Results 1 - 10 of 11 for Amyotrophic lateral sclerosis type 6
  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 article on PubMed Central
    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. ...
    https://medlineplus.gov/genetics/gene/fus - Genetics
  3. 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
  4. SETX gene 
    ... helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). Am J Hum Genet. 2004 Jun;74(6):1128-35. doi: 10.1086/421054. Epub 2004 ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  5. 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
  6. C9orf72 gene 
    ... the C9orf72 gene have been found to cause amyotrophic lateral sclerosis ... ALS. This type of mutation is called a hexanucleotide repeat expansion. ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  7. 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
  8. SMN1 gene 
    ... quickly broken down. ... a wide range of severity. There are many types of spinal muscular atrophy that differ in age ...
    https://medlineplus.gov/genetics/gene/smn1 - Genetics
  9. C19orf12 gene 
    ... to have a condition called hereditary spastic paraplegia type 43. More About This Health Condition ... TB. C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis. J Neurol. 2012 Nov;259(11):2434-9. ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics
  10. DCTN1 gene 
    ... how this mutation causes distal hereditary motor neuronopathy type VIIB. ... amyotrophic lateral sclerosis (ALS). This disorder occurs in mid- to late ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
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