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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. [electronic resource] by
- Balci, Burcu
- Uyanik, Gökhan
- Dincer, Pervin
- Gross, Claudia
- Willer, Tobias
- Talim, Beril
- Haliloglu, Göknur
- Kale, Gülsev
- Hehr, Ute
- Winkler, Jürgen
- Topaloğlu, Haluk
Producer: 20050613
In:
Neuromuscular disorders : NMD vol. 15
Availability: No items available.
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