HIGHLIGHTS
- who: Emily C. Storey and Heidi R. Fuller from the School of Pharmacy and Bioengineering, Keele University, Staffordshire , BG, UK have published the research: Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary, in the Journal: Cells 2022, 11, 4065. of 15/Dec/2022
- what: The aim of this study was to conduct a systematic review into published mutations of genes encoding NE proteins associated with the LINC complex: LMNA, LMNB1, LMNB2, EMD, TMEM43, SUN1/SUN2 and SYNE1/SYNE2, and to analyse the list . . .
If you want to have access to all the content you need to log in!
Thanks :)
If you don't have an account, you can create one here.