The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

B. Smith; S. Newhouse; A. Shatunov; C. Vance; S. Topp; L. Johson; J. Miller; Y. Lee; C. Troakes; K.M. Scott; A. Jones; I. Gray; J. Wright; T. Hortobagyi; S. Al-Sarraj; B. Rogelj; J. Powell; M. Lupton; S. lovestone; P. Sapp; M Weber; P.J. Nestor; H.J. Schelhaas; A.A. Asbroek; V. Silani; C. Gellera; f. Taroni; N. Ticozzi; L.H. van den Berg; J.H. Veldink; P. Van Damme; W. Robberecht; P.J. Shaw; J. Kirby; H. Pall; K.E. Morrison; J. de Belleroche; J.M. Vianney de Jong; F. Baas; P.M. Andersen; J.E. Landers; R.H. Jr. Brown; M.E. Weale; A. Al-Chalabi; C.E. Shaw

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

Translated title of the contribution: The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

B. Smith, S. Newhouse, A. Shatunov, C. Vance, S. Topp, L. Johson, J. Miller, Y. Lee, C. Troakes, K.M. Scott, A. Jones, I. Gray, J. Wright, T. Hortobagyi, S. Al-Sarraj, B. Rogelj, J. Powell, M. Lupton, S. lovestone, P. SappM Weber, P.J. Nestor, H.J. Schelhaas, A.A. Asbroek, V. Silani, C. Gellera, f. Taroni, N. Ticozzi, L.H. van den Berg, J.H. Veldink, P. Van Damme, W. Robberecht, P.J. Shaw, J. Kirby, H. Pall, K.E. Morrison, J. de Belleroche, J.M. Vianney de Jong, F. Baas, P.M. Andersen, J.E. Landers, R.H. Jr. Brown, M.E. Weale, A. Al-Chalabi, C.E. Shaw

Research output: Contribution to journal › Article › Academic › peer-review

Translated title of the contribution	The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder
Original language	Undefined/Unknown
Pages (from-to)	102-108
Number of pages	7
Journal	European Journal of Human Genetics
Volume	21
Issue number	1
Publication status	Published - 2013

Keywords

Econometric and Statistical Methods: General
Geneeskunde (GENK)
Geneeskunde(GENK)
Medical sciences
Bescherming en bevordering van de menselijke gezondheid

Access to Document

http://www.ncbi.nlm.nih.gov/pubmed/22692064

Cite this

Smith, B., Newhouse, S., Shatunov, A., Vance, C., Topp, S., Johson, L., Miller, J., Lee, Y., Troakes, C., Scott, K. M., Jones, A., Gray, I., Wright, J., Hortobagyi, T., Al-Sarraj, S., Rogelj, B., Powell, J., Lupton, M., lovestone, S., ... Shaw, C. E. (2013). The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder. European Journal of Human Genetics, 21(1), 102-108. http://www.ncbi.nlm.nih.gov/pubmed/22692064

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title = "The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder",

keywords = "Econometric and Statistical Methods: General, Geneeskunde (GENK), Geneeskunde(GENK), Medical sciences, Bescherming en bevordering van de menselijke gezondheid",

author = "B. Smith and S. Newhouse and A. Shatunov and C. Vance and S. Topp and L. Johson and J. Miller and Y. Lee and C. Troakes and K.M. Scott and A. Jones and I. Gray and J. Wright and T. Hortobagyi and S. Al-Sarraj and B. Rogelj and J. Powell and M. Lupton and S. lovestone and P. Sapp and M Weber and P.J. Nestor and H.J. Schelhaas and A.A. Asbroek and V. Silani and C. Gellera and f. Taroni and N. Ticozzi and \{van den Berg\}, L.H. and J.H. Veldink and \{Van Damme\}, P. and W. Robberecht and P.J. Shaw and J. Kirby and H. Pall and K.E. Morrison and \{de Belleroche\}, J. and \{Vianney de Jong\}, J.M. and F. Baas and P.M. Andersen and J.E. Landers and Brown, \{R.H. Jr.\} and M.E. Weale and A. Al-Chalabi and C.E. Shaw",

year = "2013",

language = "Undefined/Unknown",

volume = "21",

pages = "102--108",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer Nature",

number = "1",

}

Smith, B, Newhouse, S, Shatunov, A, Vance, C, Topp, S, Johson, L, Miller, J, Lee, Y, Troakes, C, Scott, KM, Jones, A, Gray, I, Wright, J, Hortobagyi, T, Al-Sarraj, S, Rogelj, B, Powell, J, Lupton, M, lovestone, S, Sapp, P, Weber, M, Nestor, PJ, Schelhaas, HJ, Asbroek, AA, Silani, V, Gellera, C, Taroni, F, Ticozzi, N, van den Berg, LH , Veldink, JH, Van Damme, P, Robberecht, W, Shaw, PJ, Kirby, J, Pall, H, Morrison, KE, de Belleroche, J, Vianney de Jong, JM, Baas, F, Andersen, PM, Landers, JE, Brown, RHJ, Weale, ME, Al-Chalabi, A & Shaw, CE 2013, 'The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder', European Journal of Human Genetics, vol. 21, no. 1, pp. 102-108. <http://www.ncbi.nlm.nih.gov/pubmed/22692064>

TY - JOUR

T1 - The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

AU - Smith, B.

AU - Newhouse, S.

AU - Shatunov, A.

AU - Vance, C.

AU - Topp, S.

AU - Johson, L.

AU - Miller, J.

AU - Lee, Y.

AU - Troakes, C.

AU - Scott, K.M.

AU - Jones, A.

AU - Gray, I.

AU - Wright, J.

AU - Hortobagyi, T.

AU - Al-Sarraj, S.

AU - Rogelj, B.

AU - Powell, J.

AU - Lupton, M.

AU - lovestone, S.

AU - Sapp, P.

AU - Weber, M

AU - Nestor, P.J.

AU - Schelhaas, H.J.

AU - Asbroek, A.A.

AU - Silani, V.

AU - Gellera, C.

AU - Taroni, f.

AU - Ticozzi, N.

AU - van den Berg, L.H.

AU - Veldink, J.H.

AU - Van Damme, P.

AU - Robberecht, W.

AU - Shaw, P.J.

AU - Kirby, J.

AU - Pall, H.

AU - Morrison, K.E.

AU - de Belleroche, J.

AU - Vianney de Jong, J.M.

AU - Baas, F.

AU - Andersen, P.M.

AU - Landers, J.E.

AU - Brown, R.H. Jr.

AU - Weale, M.E.

AU - Al-Chalabi, A.

AU - Shaw, C.E.

PY - 2013

Y1 - 2013

KW - Econometric and Statistical Methods: General

KW - Geneeskunde (GENK)

KW - Geneeskunde(GENK)

KW - Medical sciences

KW - Bescherming en bevordering van de menselijke gezondheid

M3 - Article

SN - 1018-4813

VL - 21

SP - 102

EP - 108

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 1

ER -