Distinct cerebral lesions in sporadic and ‘D90A’ SOD1 ALS: studies with [11C]flumazenil PET
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/128/6/1323/1190410/awh509.pdf
Reference40 articles.
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3. Aggarwal A, Nicholson G. Normal complement of motor units in asymptomatic familial (SOD1 mutation) amyotrophic lateral sclerosis carriers. J Neurol Neurosurg Psychiatry2001; 71: 478–81.
4. Al-Chalabi A, Andersen PM, Chioza B, et al. Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor. Hum Mol Genet1998; 7: 2045–50.
5. Andersen PM. Genetic aspects of amyotrophic lateral sclerosis/motor neuron disease. In: Shaw PJ, Strong MJ, editors. Motor neuron disease. New York: Butterworth Heinemann; 2003. p. 207–36.
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