Frontiers | The EDA/EDAR/NF-κB pathway in non-syndromic tooth agenesis: A genetic perspective
Extensii Gene by Eda Lashes | Gene False
EDA signaling pathway. The trimeric EDA ligand binds to the trimeric... | Download Scientific Diagram
Conservation analysis and pathogenicity prediction of mutant genes of ectodysplasin a | BMC Medical Genetics | Full Text
The ectodysplasin pathway: from diseases to adaptations: Trends in Genetics
EDA Gene - GeneCards | EDA Protein | EDA Antibody
Frontiers | Pathogenic EDA Mutations in Chinese Han Families With Hypohidrotic Ectodermal Dysplasia and Genotype–Phenotype: A Correlation Analysis
IJMS | Free Full-Text | Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
Frontiers | Functional and clinical analysis of five EDA variants associated with ectodermal dysplasia but with a hard-to-predict significance
Ectodysplasine — Wikipédia
A and B, EDA gene sequencing results show a (CGC > CAC) missense... | Download Scientific Diagram
Genes | Free Full-Text | Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients
A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia | Journal of Human Genetics
Genes | Free Full-Text | Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations
Identification of a novel 2-bp insertion mutation in the EDA gene. (A)... | Download Scientific Diagram
IJMS | Free Full-Text | Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
Ectodysplasin A - an overview | ScienceDirect Topics
EDA Antibodies & ELISA Kits, EDA Proteins
EDA (Gene) - an overview | ScienceDirect Topics
Figure 3 from Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia and hypodontia in Chinese kindreds. | Semantic Scholar
Gene: EDA (ENSSSCG00000021647) - Summary - Sus_scrofa - Ensembl genome browser 110
A novel frameshift mutation in the EDA gene in an Iranian patient affected by X-linked hypohidrotic ectodermal dysplasia | Cellular & Molecular Biology Letters | Full Text
