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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
Author(s) -
Nakajima Yoko,
Meijer Judith,
Dobritzsch Doreen,
Ito Tetsuya,
Meinsma Rutger,
Abeling Nico G. G. M.,
Roelofsen Jeroen,
Zoetekouw Lida,
Watanabe Yoriko,
Tashiro Kyoko,
Lee Tomoko,
Takeshima Yasuhiro,
Mitsubuchi Hiroshi,
Yoneyama Akira,
Ohta Kazuhide,
Eto Kaoru,
Saito Kayoko,
Kuhara Tomiko,
Kuilenburg André B. P.
Publication year - 2014
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/s10545-014-9754-z
Subject(s) - human genetics , mutation , genetics , medicine , bioinformatics , pediatrics , biology , gene