Journal article

The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder.

Publication status:: Published

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APA Style

Müller, J., Abicht, A., Burke, G., Cossins, J., Richard, P., Baumeister, S., Stucka, R., Eymard, B., Hantaï, D., Beeson, D., & Lochmüller, H. (2004). The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder. Journal of Medical Genetics, 41(8), e104.

MLA Style

Müller, J., et al. “The Congenital Myasthenic Syndrome Mutation RAPSN N88K Derives from an Ancient Indo-European Founder.” Journal of Medical Genetics, vol. 41, no. 8, 2004, p. e104.

Chicago Style

Müller, J, A Abicht, G Burke, J Cossins, P Richard, S Baumeister, R Stucka, et al. 2004. “The Congenital Myasthenic Syndrome Mutation RAPSN N88K Derives from an Ancient Indo-European Founder.” Journal of Medical Genetics 41 (8): e104.
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Publisher copy:: 10.1136/jmg.2004.021139

Authors

+ Müller, J More by this author

Role:: Author

+ Abicht, A More by this author

Role:: Author

+ Burke, G More by this author

Role:: Author

+ Cossins, J More by this author

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+ Richard, P More by this author

Role:: Author

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Journal:: Journal of medical genetics More from this journal
Volume:: 41
Issue:: 8
Pages:: e104
Publication date:: 2004-08-01
DOI:: 10.1136/jmg.2004.021139
EISSN:: 1468-6244
ISSN:: 0022-2593

Language:: English
Keywords:: Mutation, Missense

Evolution, Molecular

Founder Effect

Myasthenic Syndromes, Congenital

Lysine

Asparagine

Europe

Humans

Muscle Proteins

India
Pubs id:: pubs:324386
UUID:: uuid:e54ae99c-84e2-4c0f-8bc1-4e77ee24686f
Local pid:: pubs:324386
Source identifiers:: 324386
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2004

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

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