Associated Papers
Compound Heterozygous Null Variants in ITGB4 Gene Causing Severe Phenotype of Junctional Epidermolysis Bullosa With Pyloric Atresia in Thai Newborn: Genotype-Phenotype Correlation From a Case Report and Review of the Literature.
Klangjorhor J et al.
International Journal of Genomics, 2025
Whole exome sequencing approach for identification of the molecular etiology in pediatric patients with hematuria.
Wu J et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2024
Intestinal Failure in Junctional Epidermolysis Bullosa: Mild Skin Disease, Severe Diarrhea.
DeMaria KA et al.
Digestive Diseases and Sciences, 2022
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