Erratum: Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy (The American Journal of Human Genetics (2014) 95 (332-339))

David N. Herrmann; Rita Horvath; Janet E. Sowden; Michael Gonzalez; Avencia Sanchez-Mejias; Zhuo Guan; Roger G. Whittaker; Jorge L. Almodovar; Maria Lane; Boglarka Bansagi; Angela Pyle; Veronika Boczonadi; Hanns Lochmüller; Helen Griffin; Patrick F. Chinnery; Thomas E. Lloyd; J. Troy Littleton; Stephan Zuchner

doi:10.1016/j.ajhg.2014.09.012

Erratum: Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy (The American Journal of Human Genetics (2014) 95 (332-339))

David N. Herrmann, Rita Horvath, Janet E. Sowden, Michael Gonzalez, Avencia Sanchez-Mejias, Zhuo Guan, Roger G. Whittaker, Jorge L. Almodovar, Maria Lane, Boglarka Bansagi, Angela Pyle, Veronika Boczonadi, Hanns Lochmüller, Helen Griffin, Patrick F. Chinnery, Thomas E. Lloyd, J. Troy Littleton, Stephan Zuchner

School of Medicine

Research output: Contribution to journal › Comment/debate › peer-review

1 Scopus citations

Original language	English (US)
Pages (from-to)	472
Number of pages	1
Journal	American journal of human genetics
Volume	95
Issue number	4
DOIs	https://doi.org/10.1016/j.ajhg.2014.09.012
State	Published - 2014

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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Herrmann, D. N., Horvath, R., Sowden, J. E., Gonzalez, M., Sanchez-Mejias, A., Guan, Z., Whittaker, R. G., Almodovar, J. L., Lane, M., Bansagi, B., Pyle, A., Boczonadi, V., Lochmüller, H., Griffin, H., Chinnery, P. F., Lloyd, T. E., Littleton, J. T., & Zuchner, S. (2014). Erratum: Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy (The American Journal of Human Genetics (2014) 95 (332-339)). American journal of human genetics, 95(4), 472. https://doi.org/10.1016/j.ajhg.2014.09.012

Erratum: Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy (The American Journal of Human Genetics (2014) 95 (332-339)). / Herrmann, David N.; Horvath, Rita; Sowden, Janet E. et al.
In: American journal of human genetics, Vol. 95, No. 4, 2014, p. 472.

Research output: Contribution to journal › Comment/debate › peer-review

Herrmann, DN, Horvath, R, Sowden, JE, Gonzalez, M, Sanchez-Mejias, A, Guan, Z, Whittaker, RG, Almodovar, JL, Lane, M, Bansagi, B, Pyle, A, Boczonadi, V, Lochmüller, H, Griffin, H, Chinnery, PF, Lloyd, TE, Littleton, JT & Zuchner, S 2014, 'Erratum: Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy (The American Journal of Human Genetics (2014) 95 (332-339))', American journal of human genetics, vol. 95, no. 4, pp. 472. https://doi.org/10.1016/j.ajhg.2014.09.012

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author = "Herrmann, {David N.} and Rita Horvath and Sowden, {Janet E.} and Michael Gonzalez and Avencia Sanchez-Mejias and Zhuo Guan and Whittaker, {Roger G.} and Almodovar, {Jorge L.} and Maria Lane and Boglarka Bansagi and Angela Pyle and Veronika Boczonadi and Hanns Lochm{\"u}ller and Helen Griffin and Chinnery, {Patrick F.} and Lloyd, {Thomas E.} and Littleton, {J. Troy} and Stephan Zuchner",

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Erratum: Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy (The American Journal of Human Genetics (2014) 95 (332-339))

ASJC Scopus subject areas

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