Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia
M Taniguchi-Ikeda1,2, N Morisada3, H Inagaki4
1Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Clinical Genetics
|December 16, 2017
Abstract
No abstract available in PubMed .
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