Journal article

Another gene for ALS: mutations in sporadic cases and the rare variant hypothesis.

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APA Style

Talbot, K. (2009). Another gene for ALS: mutations in sporadic cases and the rare variant hypothesis. Neurology, 73(15), 1172–1173.

MLA Style

Talbot, K. “Another Gene for ALS: Mutations in Sporadic Cases and the Rare Variant Hypothesis.” Neurology, vol. 73, no. 15, 2009, pp. 1172–73.

Chicago Style

Talbot, K. 2009. “Another Gene for ALS: Mutations in Sporadic Cases and the Rare Variant Hypothesis.” Neurology 73 (15): 1172–73.
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Publisher copy:: 10.1212/wnl.0b013e3181bd1161

Authors

+ Talbot, K More by this author

Institution:: University of Oxford
Division:: MSD
Department:: Clinical Neurosciences
Role:: Author

Journal:: Neurology More from this journal
Volume:: 73
Issue:: 15
Pages:: 1172-1173
Publication date:: 2009-10-01
DOI:: 10.1212/wnl.0b013e3181bd1161
EISSN:: 1526-632X
ISSN:: 0028-3878

Language:: English
Keywords:: Family Health

Amyotrophic Lateral Sclerosis

Models, Genetic

RNA-Binding Protein FUS

Genetic Testing

Mutation

Humans
Pubs id:: pubs:245442
UUID:: uuid:61b2cc46-48d6-4890-9384-25658d61b888
Local pid:: pubs:245442
Source identifiers:: 245442
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2009

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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