Pages that link to "Q80465252"
Jump to navigation
Jump to search
The following pages link to Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families (Q80465252):
Displaying 12 items.
- Recombinant MG53 protein modulates therapeutic cell membrane repair in treatment of muscular dystrophy (Q30545559) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- Phenotypic variability in siblings with calpainopathy (LGMD2A). (Q33807663) (← links)
- Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic (Q35227523) (← links)
- Plasma Membrane Repair: A Central Process for Maintaining Cellular Homeostasis (Q36240722) (← links)
- Genetic basis of limb-girdle muscular dystrophies: the 2014 update (Q38213016) (← links)
- Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations (Q38553524) (← links)
- How to tackle the diagnosis of limb-girdle muscular dystrophy 2A (Q42271189) (← links)
- Frequency of the FKRP mutation c.826C>A in isolated hyperCKemia and in limb girdle muscular dystrophy type 2 in German patients (Q43263549) (← links)
- Left ventricular deformation abnormalities in a patient with calpainopathy-a case from the three-dimensional speckle-tracking echocardiographic MAGYAR-Path Study (Q47220229) (← links)
- Enhancing membrane repair increases regeneration in a sciatic injury model (Q91762736) (← links)
- ANO5 mutations in the Polish limb girdle muscular dystrophy patients: Effects on the protein structure (Q92509407) (← links)