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: Comment/debate査読

本文言語English
ページ(範囲)1023
ページ数1
ジャーナルJournal of Inherited Metabolic Disease
37
6
DOI
出版ステータスPublished - 23-10-2014
外部発表はい

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

引用スタイル