The p.P56S mutation in the VAPB gene is not due to a single founder: The first European case

A. D. Funke; M. Esser; A. Krüttgen; J. Weis; M. Mitne-Neto; M. Lazar; A. L. Nishimura; A. D. Sperfeld; P. Trillenberg; J. Senderek; M. Krasnianski; M. Zatz; S. Zierz; M. Deschauer

doi:10.1111/j.1399-0004.2009.01319.x

The p.P56S mutation in the VAPB gene is not due to a single founder: The first European case

A. D. Funke, M. Esser, A. Krüttgen, J. Weis, M. Mitne-Neto, M. Lazar, A. L. Nishimura, A. D. Sperfeld, P. Trillenberg, J. Senderek, M. Krasnianski, M. Zatz, S. Zierz, M. Deschauer

Research output: Contribution to journal › Letter › peer-review

50 Scopus citations

Original language	English
Pages (from-to)	302-303
Number of pages	2
Journal	Clinical Genetics
Volume	77
Issue number	3
DOIs	https://doi.org/10.1111/j.1399-0004.2009.01319.x
State	Published - Mar 2010
Externally published	Yes

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Funke, A. D., Esser, M., Krüttgen, A., Weis, J., Mitne-Neto, M., Lazar, M., Nishimura, A. L., Sperfeld, A. D., Trillenberg, P., Senderek, J., Krasnianski, M., Zatz, M., Zierz, S., & Deschauer, M. (2010). The p.P56S mutation in the VAPB gene is not due to a single founder: The first European case. Clinical Genetics, 77(3), 302-303. https://doi.org/10.1111/j.1399-0004.2009.01319.x

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title = "The p.P56S mutation in the VAPB gene is not due to a single founder: The first European case",

author = "Funke, {A. D.} and M. Esser and A. Kr{\"u}ttgen and J. Weis and M. Mitne-Neto and M. Lazar and Nishimura, {A. L.} and Sperfeld, {A. D.} and P. Trillenberg and J. Senderek and M. Krasnianski and M. Zatz and S. Zierz and M. Deschauer",

year = "2010",

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doi = "10.1111/j.1399-0004.2009.01319.x",

language = "English",

volume = "77",

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Funke, AD, Esser, M, Krüttgen, A, Weis, J, Mitne-Neto, M, Lazar, M, Nishimura, AL, Sperfeld, AD, Trillenberg, P, Senderek, J, Krasnianski, M, Zatz, M, Zierz, S & Deschauer, M 2010, 'The p.P56S mutation in the VAPB gene is not due to a single founder: The first European case', Clinical Genetics, vol. 77, no. 3, pp. 302-303. https://doi.org/10.1111/j.1399-0004.2009.01319.x

TY - JOUR

T1 - The p.P56S mutation in the VAPB gene is not due to a single founder

T2 - The first European case

AU - Funke, A. D.

AU - Esser, M.

AU - Krüttgen, A.

AU - Weis, J.

AU - Mitne-Neto, M.

AU - Lazar, M.

AU - Nishimura, A. L.

AU - Sperfeld, A. D.

AU - Trillenberg, P.

AU - Senderek, J.

AU - Krasnianski, M.

AU - Zatz, M.

AU - Zierz, S.

AU - Deschauer, M.

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U2 - 10.1111/j.1399-0004.2009.01319.x

DO - 10.1111/j.1399-0004.2009.01319.x

M3 - Letter

C2 - 20447143

AN - SCOPUS:77950170203

SN - 0009-9163

VL - 77

SP - 302

EP - 303

JO - Clinical Genetics

JF - Clinical Genetics

IS - 3

ER -

The p.P56S mutation in the VAPB gene is not due to a single founder: The first European case

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