Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations - Vainzof, Mariz; Marie, Suely Kazue Nagahashi; Reed, Umbertina Conti; Schwartzman, J S; Pavanello, R C M; Passos-Bueno, Maria Rita; Zatz, Mayana (Neuropediatrics, 1995)