Epidermolysis Bullosa: Two rare case reports of COL7A1 and EBS-GEN SEV KRT14 variants with review of literature

Abstract Epidermolysis Bullosa is a rare hereditary skin condition that causes blisters. Genes encoding structural proteins at or near the dermal-epidermal junction are mutated recessively or dominantly, and this is the primary cause of EB. Herein, two Chinese boys were diagnosed with the condition,...

Full description

Saved in:
Bibliographic Details
Main Authors: Fatma Mabrouk Ali (Author), Jieyu Zhou (Author), Mingyan Wang (Author), Qiuxia Wang (Author), Lulu Sun (Author), Mansour Maulid Mshenga (Author), Hongyan Lu (Author)
Format: Book
Published: BMC, 2024-04-01T00:00:00Z.
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