| 1 | FKRP, FKTN, ITGA7, ITGA7D, LAMA2, MDC1A, MDC1B, POMGNT1, POMT1, RSMD1, SEPN1, WLKWS1, WLKWS4 |
| Case 35-2006 -- A Newborn Boy with Hypotonia. | |
| Brown RH Jr, Grant PE, Pierson CR. | |
| N Engl J Med 355(20):2132-2142. No abstract available. 2006 | |
| 2 | MDC1B |
| Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42. | |
| Brockington M, Sewry CA, Herrmann R, Naom I, Dearlove A, Rhodes M, Topaloglu H, Dubowitz V, Voit T, Muntoni F. | |
| Am J Hum Genet 66(2):428-35. 2000 | |