Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y)

Yoko Nakajima; Judith Meijer; Doreen Dobritzsch; Tetsuya Ito; Rutger Meinsma; Nico G.G.M. Abeling; Jeroen Roelofsen; Lida Zoetekouw; Yoriko Watanabe; Kyoko Tashiro; Tomoko Lee; Yasuhiro Takeshima; Hiroshi Mitsubuchi; Akira Yoneyama; Kazuhide Ohta; Kaoru Eto; Kayoko Saito; Tomiko Kuhara; André B.P. van Kuilenburg

doi:10.1007/s10545-014-9754-z

Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y)

Yoko Nakajima
, Judith Meijer
, Doreen Dobritzsch
, Tetsuya Ito
, Rutger Meinsma
, Nico G.G.M. Abeling
, Jeroen Roelofsen
, Lida Zoetekouw
, Yoriko Watanabe
, Kyoko Tashiro
, Tomoko Lee
, Yasuhiro Takeshima
, Hiroshi Mitsubuchi
, Akira Yoneyama
, Kazuhide Ohta
, Kaoru Eto
, Kayoko Saito
, Tomiko Kuhara
, André B.P. van Kuilenburg

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

Original language	English
Pages (from-to)	1023
Number of pages	1
Journal	Journal of Inherited Metabolic Disease
Volume	37
Issue number	6
DOIs	https://doi.org/10.1007/s10545-014-9754-z
Publication status	Published - 23-10-2014
Externally published	Yes

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)

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10.1007/s10545-014-9754-z

Cite this

Nakajima, Y., Meijer, J., Dobritzsch, D., Ito, T., Meinsma, R., Abeling, N. G. G. M., Roelofsen, J., Zoetekouw, L., Watanabe, Y., Tashiro, K., Lee, T., Takeshima, Y., Mitsubuchi, H., Yoneyama, A., Ohta, K., Eto, K., Saito, K., Kuhara, T., & van Kuilenburg, A. B. P. (2014). Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y). Journal of Inherited Metabolic Disease, 37(6), 1023. https://doi.org/10.1007/s10545-014-9754-z

Nakajima, Yoko ; Meijer, Judith ; Dobritzsch, Doreen et al. / Erratum to : Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y). In: Journal of Inherited Metabolic Disease. 2014 ; Vol. 37, No. 6. pp. 1023.

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title = "Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y)",

author = "Yoko Nakajima and Judith Meijer and Doreen Dobritzsch and Tetsuya Ito and Rutger Meinsma and Abeling, \{Nico G.G.M.\} and Jeroen Roelofsen and Lida Zoetekouw and Yoriko Watanabe and Kyoko Tashiro and Tomoko Lee and Yasuhiro Takeshima and Hiroshi Mitsubuchi and Akira Yoneyama and Kazuhide Ohta and Kaoru Eto and Kayoko Saito and Tomiko Kuhara and \{van Kuilenburg\}, \{Andr{\'e} B.P.\}",

year = "2014",

month = oct,

day = "23",

doi = "10.1007/s10545-014-9754-z",

language = "English",

volume = "37",

pages = "1023",

journal = "Journal of Inherited Metabolic Disease",

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publisher = "Springer Netherlands",

number = "6",

}

Nakajima, Y, Meijer, J, Dobritzsch, D, Ito, T, Meinsma, R, Abeling, NGGM, Roelofsen, J, Zoetekouw, L, Watanabe, Y, Tashiro, K, Lee, T, Takeshima, Y, Mitsubuchi, H, Yoneyama, A, Ohta, K, Eto, K, Saito, K, Kuhara, T & van Kuilenburg, ABP 2014, 'Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y)', Journal of Inherited Metabolic Disease, vol. 37, no. 6, pp. 1023. https://doi.org/10.1007/s10545-014-9754-z

Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y). / Nakajima, Yoko; Meijer, Judith; Dobritzsch, Doreen et al.
In: Journal of Inherited Metabolic Disease, Vol. 37, No. 6, 23.10.2014, p. 1023.

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

TY - JOUR

T1 - Erratum to

T2 - Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y)

AU - Nakajima, Yoko

AU - Meijer, Judith

AU - Dobritzsch, Doreen

AU - Ito, Tetsuya

AU - Meinsma, Rutger

AU - Abeling, Nico G.G.M.

AU - Roelofsen, Jeroen

AU - Zoetekouw, Lida

AU - Watanabe, Yoriko

AU - Tashiro, Kyoko

AU - Lee, Tomoko

AU - Takeshima, Yasuhiro

AU - Mitsubuchi, Hiroshi

AU - Yoneyama, Akira

AU - Ohta, Kazuhide

AU - Eto, Kaoru

AU - Saito, Kayoko

AU - Kuhara, Tomiko

AU - van Kuilenburg, André B.P.

PY - 2014/10/23

Y1 - 2014/10/23

UR - https://www.scopus.com/pages/publications/84911994923

UR - https://www.scopus.com/pages/publications/84911994923#tab=citedBy

U2 - 10.1007/s10545-014-9754-z

DO - 10.1007/s10545-014-9754-z

M3 - Comment/debate

AN - SCOPUS:84911994923

SN - 0141-8955

VL - 37

SP - 1023

JO - Journal of Inherited Metabolic Disease

JF - Journal of Inherited Metabolic Disease

IS - 6

ER -

Nakajima Y, Meijer J, Dobritzsch D, Ito T, Meinsma R, Abeling NGGM et al. Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y). Journal of Inherited Metabolic Disease. 2014 Oct 23;37(6):1023. doi: 10.1007/s10545-014-9754-z

Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y)

All Science Journal Classification (ASJC) codes

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