Pages that link to "Q57398255"
Jump to navigation
Jump to search
The following pages link to Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families (Q57398255):
Displaying 21 items.
- Limb-girdle Muscular Dystrophies in India: A Review (Q33795491) (← links)
- Redox state and mitochondrial respiratory chain function in skeletal muscle of LGMD2A patients (Q33981877) (← links)
- Limb-girdle muscular dystrophy subtypes: First-reported cohort from northeastern China (Q34094843) (← links)
- Mutations of CAPN3 in Korean patients with limb-girdle muscular dystrophy (Q37220537) (← links)
- Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle (Q37295056) (← links)
- Therapeutic possibilities in the autosomal recessive limb-girdle muscular dystrophies (Q37329558) (← links)
- Failure to up-regulate transcription of genes necessary for muscle adaptation underlies limb girdle muscular dystrophy 2A (calpainopathy). (Q37367980) (← links)
- Calpainopathy-a survey of mutations and polymorphisms (Q42036972) (← links)
- How to tackle the diagnosis of limb-girdle muscular dystrophy 2A (Q42271189) (← links)
- Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy (Q50991485) (← links)
- Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan (Q51980072) (← links)
- (Q58194591) (redirect page) (← links)
- The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients (Q58782428) (← links)
- (Q61968043) (redirect page) (← links)
- (Q62937443) (redirect page) (← links)
- Limb girdle muscular dystrophy type 2A presenting with cardiac arrest (Q73746113) (← links)
- Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy (Q74432097) (← links)
- Electrodiagnostic approach to the patient with suspected myopathy (Q74552809) (← links)
- (Q77407600) (redirect page) (← links)
- C3KO mouse expression analysis: downregulation of the muscular dystrophy Ky protein and alterations in muscle aging (Q84596582) (← links)
- Usefulness of comprehensive targeted multigene panel sequencing for neuromuscular disorders in Korean patients (Q93050552) (← links)