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Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?
J Neurol Neurosurg Psychiatry. 2010 May;81(5):572-7. doi: 10.1136/jnnp.2009.192310.
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Mutations of optineurin in amyotrophic lateral sclerosis.
Nature. 2010 May 13;465(7295):223-6. doi: 10.1038/nature08971. Epub 2010 Apr 28.
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Disclosure of APOE genotype for risk of Alzheimer's disease.
N Engl J Med. 2009 Jul 16;361(3):245-54. doi: 10.1056/NEJMoa0809578.
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Telephoned BRCA1/2 genetic test results: prevalence, practice, and patient satisfaction.
J Genet Couns. 2009 Oct;18(5):447-63. doi: 10.1007/s10897-009-9238-8. Epub 2009 May 22.
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Mutations 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.
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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
Science. 2009 Feb 27;323(5918):1205-8. doi: 10.1126/science.1166066.
7
Long-term outcome of presymptomatic testing in Huntington disease.
Eur J Hum Genet. 2009 Feb;17(2):165-71. doi: 10.1038/ejhg.2008.146. Epub 2008 Aug 20.
8
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.
Lancet Neurol. 2008 May;7(5):409-16. doi: 10.1016/S1474-4422(08)70071-1. Epub 2008 Apr 7.
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Prevalence of SOD1 mutations in the Italian ALS population.
Neurology. 2008 Feb 12;70(7):533-7. doi: 10.1212/01.wnl.0000299187.90432.3f.
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Living at risk: concealing risk and preserving hope in Huntington disease.
J Genet Couns. 2008 Feb;17(1):117-28. doi: 10.1007/s10897-007-9133-0. Epub 2007 Oct 18.

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