Pages that link to "Q58052166"
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The following pages link to Calpain-3 mutations in Turkey (Q58052166):
Displaying 13 items.
- Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review). (Q33608787) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- Limb-girdle Muscular Dystrophies in India: A Review (Q33795491) (← links)
- Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies. (Q36007760) (← links)
- Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations. (Q37004486) (← links)
- Therapeutic possibilities in the autosomal recessive limb-girdle muscular dystrophies (Q37329558) (← links)
- Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: The yield and the pitfalls (Q38434135) (← links)
- Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group (Q40718887) (← links)
- How to tackle the diagnosis of limb-girdle muscular dystrophy 2A (Q42271189) (← links)
- cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark (Q50547039) (← links)
- Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia (Q91589129) (← links)
- Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey (Q92152493) (← links)
- Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients (Q104283370) (← links)