Junctional epidermolysis bullosa gravis (Herlitz): diagnostic and genetic aspects
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1468-3083.2001.00215.x/fullpdf
Reference14 articles.
1. Revised classification system for inherited epidermolysis bullosa
2. Digenic Junctional Epidermolysis Bullosa: Mutations in COL17A1 and LAMB3 Genes
3. Junctional epidermolysis bullosa: Diagnosis and management of a patient with the Herlitz variant
4. Prenatal diagnosis of herlitz junctional epidermolysis bullosa by amniocentesis
5. Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: Implications for prenatal diagnosis in one family
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1. Epidermólisis bullosa en España: Estudio observacional de una cohorte de pacientes atendidos en un centro de referencia nacional;Actas Dermo-Sifiliográficas;2021-10
2. Epidermolysis Bullosa in Spain: Observational Study of a Cohort of Patients Treated in a National Referral Center;Actas Dermo-Sifiliográficas (English Edition);2021-10
3. Targeted next-generation sequencing identifies a novel mutation of LAMB3 in a Chinese neonatal patient presented with junctional epidermolysis bullosa;Medicine;2018-12
4. Epidermolysis bullosa in animals: a review;Veterinary Dermatology;2014-10-30
5. Epidermólisis bullosa de Herlitz en el paciente pediátrico: implicaciones anestésicas;Revista Colombiana de Anestesiología;2014-04
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