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

研究成果: ジャーナルへの寄稿 › コメント/討論 › 査読

本文言語	英語
ページ（範囲）	1023
ページ数	1
ジャーナル	Journal of Inherited Metabolic Disease
巻	37
号	6
DOI	https://doi.org/10.1007/s10545-014-9754-z
出版ステータス	出版済み - 23-10-2014
外部発表	はい

All Science Journal Classification (ASJC) codes

遺伝学
遺伝学（臨床）

文献へのアクセス

10.1007/s10545-014-9754-z

他のファイルとリンク

引用スタイル

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 その他. / 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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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.}",

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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 その他.
In: Journal of Inherited Metabolic Disease, Vol. 37, No. 6, 23.10.2014, p. 1023.

研究成果: ジャーナルへの寄稿 › コメント/討論 › 査読

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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

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Nakajima Y, Meijer J, Dobritzsch D, Ito T, Meinsma R, Abeling NGGM その他. 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 10月 23;37(6):1023. doi: 10.1007/s10545-014-9754-z