Kelch-like family member 40 deficiency effect on the skeletal muscle
Transcriptomics Dataset
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General Information
| Accession | GSE56570 |
| Title | Kelch-like family member 40 deficiency effect on the skeletal muscle |
| Description | Analysis of quadriceps muscles of mutants lacking kelch-like family member 40 (KLHL40). KLHL40 mutations occur in severe nemaline myopathies (NMs). NMs are congenital myopathies that can result in lethal muscle dysfunction. Results provide insight into the role of KLHL40 in the pathogenesis of NM. |
| Landing Page | https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE56570 |
| Repository | Gene Expression Omnibus |
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