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A Recurrent Loss-of-Function Alanyl-tRNA Synthetase (AARS) Mutation in Patients with Charcot-Marie-Tooth Disease Type 2N (CMT2N)

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APA Style

Mclaughlin, H., Sakaguchi, R., Giblin, W., Wilson, T., Biesecker, L., Lupski, J. R., Talbot, K., Vance, J., Züchner, S., Lee, Y., Kennerson, M., Hou, Y., Nicholson, G., & Antonellis, A. (2014). A Recurrent Loss-of-Function Alanyl-tRNA Synthetase (AARS) Mutation in Patients with Charcot-Marie-Tooth Disease Type 2N (CMT2N). Human Mutation, 35(4), 512–512.

MLA Style

Mclaughlin, H, et al. “A Recurrent Loss-of-Function Alanyl-TRNA Synthetase (AARS) Mutation in Patients with Charcot-Marie-Tooth Disease Type 2N (CMT2N).” Human Mutation, vol. 35, no. 4, 2014, pp. 512–12.

Chicago Style

Mclaughlin, H, R Sakaguchi, W Giblin, et al. 2014. “A Recurrent Loss-of-Function Alanyl-TRNA Synthetase (AARS) Mutation in Patients with Charcot-Marie-Tooth Disease Type 2N (CMT2N).” Human Mutation 35 (4): 512–12.
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Publisher copy:: 10.1002/humu.22527

Authors

+ Mclaughlin, H More by this author

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+ Sakaguchi, R More by this author

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+ Giblin, W More by this author

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+ Wilson, T More by this author

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+ Biesecker, L More by this author

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Publisher:: Wiley-Liss Inc.
Journal:: Human Mutation More from this journal
Volume:: 35
Issue:: 4
Pages:: 512-512
Publication date:: 2014-01-01
DOI:: 10.1002/humu.22527
EISSN:: 1098-1004
ISSN:: 1059-7794

Language:: English
Pubs id:: pubs:474873
UUID:: uuid:bcd5236e-ebd0-4d39-a4e9-e896ad5306b0
Local pid:: pubs:474873
Source identifiers:: 474873
Deposit date:: 2014-07-11
ARK identifier:: ark:/29072/ora_bcd5236eebd04d39a4e9e896ad5306b0

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Copyright date:: 2014

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

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