Biallelic mutations in SZT2 cause a discernible clinical...

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Brain and Development 2017 / 10

Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum

Nakamura, Yuji, Togawa, Yasuko, Okuno, Yusuke, Muramatsu, Hideki, Nakabayashi, Kazuhiko, Kuroki, Yoko, Ieda, Daisuke, Hori, Ikumi, Negishi, Yutaka, Togawa, Takao, Hattori, Ayako, Kojima, Seiji, Saitoh
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Language:
english
Journal:
Brain and Development
DOI:
10.1016/j.braindev.2017.08.003
Date:
October, 2017
File:
PDF, 934 KB
english, 2017
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