An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker–Warburg syndrome (WWS) caused by a mutation in the POMT1 gene
| Autor: | Balci, Burcu, Uyanik, Gökhan, Dincer, Pervin, Gross, Claudia, Willer, Tobias, Talim, Beril, Haliloglu, Göknur, Kale, Gülsev, Hehr, Ute, Winkler, Jürgen, Topaloğlu, Haluk |
|---|---|
| Zdroj: | In Neuromuscular Disorders 2005 15(4):271-275 |
| Databáze: | ScienceDirect |
| Externí odkaz: |
|
Full Text from ScienceDirect