AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical modelRuizhi Deng, Reza Maroofian, Eva Medico Salsench et al.|Acta Neuropathologica|2023Cited by 22
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous PopulationMohammad A. Al–Muhaizea, Namik Kaya, Wafa Alotaibi et al.|Genes|2021Cited by 8