Cite
HARVARD Citation
Taniguchi‐Ikeda, M. et al. (2018). Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia. Clinical genetics. 93 (4), pp. 931-933. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Taniguchi‐Ikeda, M. et al. (2018). Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia. Clinical genetics. 93 (4), pp. 931-933. [Online].