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Results 1 - 10 of 12 for Amyotrophic lateral sclerosis type 4
  1. Charcot-Marie-Tooth disease 
    ... the nerve impulse. People with CMT2 may develop amyotrophic lateral ... myelin and axons. Type 4 (CMT4) is distinguished from the other types by ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  2. Amyotrophic lateral sclerosis 
    ... SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8 AMYOTROPHIC ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  3. FUS gene 
    ... in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science. 2009 Feb 27;323(5918):1208- ...
    https://medlineplus.gov/genetics/gene/fus - 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. 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) ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  6. SETX gene 
    ... of damaged DNA. MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition At least 125 mutations in the SETX gene have been found to cause ataxia with oculomotor apraxia type 2. This condition is characterized by difficulty coordinating ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  7. SOD1 gene 
    ... j.bbadis.2006.03.008. Epub 2006 Apr 4. Citation on PubMed ... lateral sclerosis genetics: novel SOD1 and FUS variants. Neurobiol Aging. ...
    https://medlineplus.gov/genetics/gene/sod1 - Genetics
  8. C19orf12 gene 
    ... in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral ... Clin Genet. 2013 Oct;84(4):350-5. doi: 10.1111/cge.12079. Epub ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics
  9. 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
  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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