A Novel Mutation of KRT14 Gene in a Newborn With Epidermolysis Bullosa Simplex (Dowling-Meara Type): Case Report

Perinatology
doi 10.14734/pn.2020.31.1.39
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Korean Society of Perinatology

Related search

Recessive Epidermolysis Bullosa Simplex- A Case Report

Jos Journal of Medicine
2010English

A Novel KRT5 Mutation Associated With Generalized Severe Epidermolysis Bullosa Simplex in a 2-Year-Old Chinese Boy

Experimental and Therapeutic Medicine
MedicineCancer ResearchImmunologyMicrobiology
2016English

Epidermolysis Bullosa Simplex

2020English

Epidermolysis Bullosa Simplex With Mottled Pigmentation: The First Slovenian Case

Acta Dermatovenerologica Alpina, Panonica et Adriatica
DermatologyMedicineInfectious Diseases
2014English

Epidermolysis Bullosa Simplex, Generalized Intermediate

2020English

Case Report: Whole Exome Sequencing Reveals a Novel Frameshift Deletion Mutation p.G2254fs in COL7A1 Associated With Autosomal Recessive Dystrophic Epidermolysis Bullosa

F1000Research
GeneticsMolecular BiologyPharmacologyBiochemistryMicrobiology ImmunologyMedicineToxicologyPharmaceutics
2016English

Epidermolysis Bullosa Simplex With Circinate Migratory Erythema

2020English

Case Report on Epidermolysis Bullosa Acquisita

World Journal of Current Medical and Pharmaceutical Research
2020English

Known and Novel Mutations Responsible for Epidermolysis Bullosa Simplex Cases in a Chinese Population

Experimental and Therapeutic Medicine
MedicineCancer ResearchImmunologyMicrobiology
2019English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy