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A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs, and limb ataxia

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RepOD Repository for Open Data2022-11-04 更新2026-07-23 收录
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Pokrzywa Wojciech, 2022, "A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs, and limb ataxia", https://doi.org/10.18150/9TQUTI, RepOD, V1

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2022-11-04
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