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International Institute of Molecular and Cell Biology in Warsaw

(Międzynarodowy Instytut Biologii Molekularnej i Komórkowej)

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License: CC0 Creative Commons Zero 1.0 Publication Date: 2022

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DatasetA novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs, and limb ataxia Nov 4, 2022 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

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

Nov 4, 2022

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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