Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1 q42. - Brockington,M.; Sewry,C.A.; Herrmann,R.; Naom,I.; Dearlove,A.; Rhodes,M.; Topaloglu,H.; Dubowitz,V.; Voit,T.; Muntoni,F. (Am J Hum Genet, 2000)