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    Two novel heterozygous variants in ATP1A3 cause movement disorders

    Two novel heterozygous variants in ATP1A3 cause movement disorders by Shogo Furukawa, Sachiko Miyamoto, Shinobu Fukumura, Kazuo Kubota, Toshiaki Taga, Mitsuko Nakashima, Hirotomo Saitsu

    Published 2022-02-01
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