Innovative Therapies in Genetic Diseases: Cystic Fibrosis

Cystic fibrosis, also named mucoviscidosis, is the most frequent hereditary pulmonary disease and is produced by mutations in the CFTR gene, encoding an anionic channel for chloride and bicarbonate involved in the regulation of salt and bicarbonate metabolisms. Currently, about half of the patients...

Full description

Saved in:
Bibliographic Details
Main Authors: Elena-Silvia Shelby (Author), Florina Mihaela Nedelea (Author), Tanser Huseyinoglu (Author), Relu Cocos (Author), Mihaela Badina (Author), Corina Sporea (Author), Liliana Padure (Author), Andrada Mirea (Author)
Format: Book
Published: Amaltea Medical Publishing House, 2021-03-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available