Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum
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S. Saitoh | Y. Okuno | S. Kojima | K. Nakabayashi | H. Muramatsu | A. Hattori | Yoko Kuroki | Yuji Nakamura | D. Ieda | Ikumi Hori | Yutaka Negishi | Takao Togawa | Yasuko Togawa