Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary

Mutations in genes encoding proteins associated with the linker of nucleoskeleton and cytoskeleton (LINC) complex within the nuclear envelope cause different diseases with varying phenotypes including skeletal muscle, cardiac, metabolic, or nervous system pathologies. There is some understanding of...

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Detalles Bibliográficos
Autores principales: Storey, Emily C., Fuller, Heidi R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777268/
https://www.ncbi.nlm.nih.gov/pubmed/36552829
http://dx.doi.org/10.3390/cells11244065

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777268/
https://www.ncbi.nlm.nih.gov/pubmed/36552829
http://dx.doi.org/10.3390/cells11244065

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