Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling. - Holtz AM; VanCoillie R; Vansickle EA; Carere DA; Withrow K; Torti E; Juusola J; Millan F; Person R; Guillen Sacoto MJ; Si Y; Wentzensen IM; et al. (Genetics in medicine : official journal of the American College of Medical Genetics, 2022)