Erratum to Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome [Am J Med Genet Part A, 161A, (2014) 1638-1646]

Christopher A. Chapleau; Jane Lane; Susan Kirwin; Carolyn Schanen; Kathy M.B. Vinette; Danielle Stubbolo; Patrick Macleod; Daniel G. Glaze; Kathleen J. Motil; Jeffrey L. Neul; Steven A. Skinner; Walter E. Kaufmann; Alan K. Percy

doi:10.1002/ajmg.a.36493

Erratum to Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome [Am J Med Genet Part A, 161A, (2014) 1638-1646]

Christopher A. Chapleau, Jane Lane, Susan Kirwin, Carolyn Schanen, Kathy M.B. Vinette, Danielle Stubbolo, Patrick Macleod, Daniel G. Glaze, Kathleen J. Motil, Jeffrey L. Neul, Steven A. Skinner, Walter E. Kaufmann, Alan K. Percy

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

Original language	English (US)
Pages (from-to)	1346
Number of pages	1
Journal	American Journal of Medical Genetics, Part A
Volume	164
Issue number	5
DOIs	https://doi.org/10.1002/ajmg.a.36493
State	Published - May 2014
Externally published	Yes

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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Chapleau, C. A., Lane, J., Kirwin, S., Schanen, C., Vinette, K. M. B., Stubbolo, D., Macleod, P., Glaze, D. G., Motil, K. J., Neul, J. L., Skinner, S. A., Kaufmann, W. E., & Percy, A. K. (2014). Erratum to Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome [Am J Med Genet Part A, 161A, (2014) 1638-1646]. American Journal of Medical Genetics, Part A, 164(5), 1346. https://doi.org/10.1002/ajmg.a.36493

Erratum to Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome [Am J Med Genet Part A, 161A, (2014) 1638-1646]. / Chapleau, Christopher A.; Lane, Jane; Kirwin, Susan et al.
In: American Journal of Medical Genetics, Part A, Vol. 164, No. 5, 05.2014, p. 1346.

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

Chapleau, CA, Lane, J, Kirwin, S, Schanen, C, Vinette, KMB, Stubbolo, D, Macleod, P, Glaze, DG, Motil, KJ, Neul, JL, Skinner, SA, Kaufmann, WE & Percy, AK 2014, 'Erratum to Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome [Am J Med Genet Part A, 161A, (2014) 1638-1646]', American Journal of Medical Genetics, Part A, vol. 164, no. 5, pp. 1346. https://doi.org/10.1002/ajmg.a.36493

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title = "Erratum to Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome [Am J Med Genet Part A, 161A, (2014) 1638-1646]",

author = "Chapleau, {Christopher A.} and Jane Lane and Susan Kirwin and Carolyn Schanen and Vinette, {Kathy M.B.} and Danielle Stubbolo and Patrick Macleod and Glaze, {Daniel G.} and Motil, {Kathleen J.} and Neul, {Jeffrey L.} and Skinner, {Steven A.} and Kaufmann, {Walter E.} and Percy, {Alan K.}",

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AU - Lane, Jane

AU - Kirwin, Susan

AU - Schanen, Carolyn

AU - Vinette, Kathy M.B.

AU - Stubbolo, Danielle

AU - Macleod, Patrick

AU - Glaze, Daniel G.

AU - Motil, Kathleen J.

AU - Neul, Jeffrey L.

AU - Skinner, Steven A.

AU - Kaufmann, Walter E.

AU - Percy, Alan K.

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Erratum to Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome [Am J Med Genet Part A, 161A, (2014) 1638-1646]

ASJC Scopus subject areas

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