_:vb50946095 . _:vb50946095 . _:vb50946095 "A neuroacanthocytosis characterized by absence of red blood cell Kx antigen, weak expression of Kell red blood cell antigens, acanthocytosis, compensated hemolysis, and involuntary movements that has_material_basis_in mutation in XK on chromosome Xp21.1."^^ . _:vb50946095 . _:vb50946095 "url:https://medlineplus.gov/genetics/condition/mcleod-neuroacanthocytosis-syndrome/"^^ . _:vb50946095 . _:vb50946095 . _:vb50946095 "url:https://pubmed.ncbi.nlm.nih.gov/17683354/"^^ . _:vb50946095 "url:https://pubmed.ncbi.nlm.nih.gov/8004674/"^^ . _:vb50946095 .