| 1 | DAG1, DEL3P21 |
| Heterozygous deletion of a 2-Mb region including the dystroglycan gene in a patient with mild myopathy, facial hypotonia, oral-motor dyspraxia and white matter abnormalities. | |
| Frost AR, Böhm SV, Sewduth RN, Josifova D, Ogilvie CM, Izatt L, Roberts RG. | |
| Eur J Hum Genet 18(7):852-5. Epub 2010 Mar 17.PMID: 20234391 2010 | |