Dubey AA, Krygier M, Szulc NA, et al. A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia. Hum Mol Genet. 2023;32(7):1152–1161. PMID: 36336956.
FEM1CFEM1CDubey AA, Krygier M, Szulc NA, et al. A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia. Hum Mol Genet. 2023;32(7):1152–1161. PMID: 36336956.