Loading...
Genotype-phenotype analysis of LMNA-related diseases predicts phenotype-selective alterations in lamin phosphorylation
Laminopathies are rare diseases associated with mutations in LMNA, which encodes nuclear lamin A/C. LMNA variants lead to diverse tissue-specific phenotypes including cardiomyopathy, lipodystrophy, myopathy, neuropathy, progeria, bone/skin disorders, and overlap syndromes. The mechanisms underlying...
Na minha lista:
| Udgivet i: | FASEB J |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2020
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8059629/ https://ncbi.nlm.nih.gov/pubmed/32413188 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.202000500R |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|