Pages that link to "Q33943919"
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The following pages link to Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE. (Q33943919):
Displaying 7 items.
- Mutation update for GNE gene variants associated with GNE myopathy. (Q34231117) (← links)
- GNE myopathy: current update and future therapy. (Q35383020) (← links)
- Prevalence of GNE p.M712T and hereditary inclusion body myopathy (HIBM) in Sangesar population of Northern Iran. (Q45990181) (← links)
- Phenotypic stratification and genotype-phenotype correlation in a heterogeneous, international cohort of GNE myopathy patients: First report from the GNE myopathy Disease Monitoring Program, registry portion (Q47204026) (← links)
- Inclusion body myositis - pathomechanism and lessons from genetics. (Q53816848) (← links)
- GNE Myopathy: Etiology, Diagnosis, and Therapeutic Challenges (Q58600532) (← links)
- Quantitative nuclear magnetic resonance imaging detects subclinical changes over 1 year in skeletal muscle of GNE myopathy (Q90736942) (← links)