Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Testing Mutation Consequences in Dystrophic Epidermolysis Bullosa

Dystrophic epidermolysis bullosa (DEB) is an inheritable blistering disease caused by mutations in COL7A1, which encodes type VII collagen. To address the issue of genotype-phenotype correlations in DEB, analyzing the consequences of COL7A1 mutations using mRNA is indispensable. Herein we establishe...

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Detalles Bibliográficos
Autores principales: Akasaka, Eijiro, Nakano, Hajime, Sawamura, Daisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709150/
https://www.ncbi.nlm.nih.gov/pubmed/34948168
http://dx.doi.org/10.3390/ijms222413369

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709150/
https://www.ncbi.nlm.nih.gov/pubmed/34948168
http://dx.doi.org/10.3390/ijms222413369

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