A Japanese case of β-ureidopropionase deficiency with dysmorphic features.
Akiyama T, Shibata T, Yoshinaga H, Kuhara T, Nakajima Y, Kato T, Maeda Y, Ohse M, Oka M, Kageyama M, Kobayashi K.
Akiyama T, et al. Among authors: ohse m.
Brain Dev. 2017 Jan;39(1):58-61. doi: 10.1016/j.braindev.2016.08.001. Epub 2016 Aug 21.
Brain Dev. 2017.
PMID: 27553092