A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia
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R. Płoski | M. Rydzanicz | W. Pokrzywa | J. Kosińska | T. Kmieć | A. Pollak | M. Mazurkiewicz-Bełdzińska | K. Rutkowska | M. Krygier | A. Dubey | N. Szulc