Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleTwo patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia.AuthorsTaniguchi‐ikeda, M.; Morisada, N.; Inagaki, H.; Ouchi, Y.; Takami, Y.; Tachikawa, M.; Satake, W.; Kobayashi, K.; Tsuneishi, S.; Takada, S.; Yamaguchi, H.; Nagase, H.; Nozu, K.; Okamoto, N.; Nishio, H.; Toda, T.; Morioka, I.; Wada, H.; Kurahashi, H.; Iijima, K.SubjectsGENETIC mutation; MICROCEPHALYPublicationClinical Genetics, 2018, Vol 93, Issue 4, p931ISSN0009-9163Publication typeLetter to the EditorDOI10.1111/cge.13106