Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant
New TNXB Mutation in EDS Patient May Be Cause of Rare Lung Collapse
Genes | Free Full-Text | Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant
Salt-wasting congenital adrenal hyperplasia phenotype as a result of the TNXA/TNXB chimera 1 (CAH-X CH-1) and the pathogenic IVS2-13A/C > G in CYP21A2 gene | Hormones
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population | Journal of Human Genetics
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Frontiers | Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome
High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia - ScienceDirect
Differentially methylated region identified within tenascin X (TNXB).... | Download Scientific Diagram
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition | Nature Genetics
Frontiers | Tenascin-X—Discovery and Early Research
Schematic diagram of CYP21A1P/CYP21A2 and TNXA/TNXB chimera genes. (A)... | Download Scientific Diagram
Classical-like Ehlers-Danlos Linked to Newly ID'd Mutation in TNXB Gene
Biallelic CAH-X genetics and phenotypes. A: TNXB variants found on the... | Download Scientific Diagram
The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers–Danlos Syndrome with 21-Hydroxylase Deficiency
Schematic diagram of CYP21A1P/CYP21A2 and TNXA/TNXB chimera genes. (A)... | Download Scientific Diagram
Frontiers | Genes and Pseudogenes: Complexity of the RCCX Locus and Disease
Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Frontiers | Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome
PDF) A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia
Missense mutations in TNXB as a cause of VUR. (A) Exons and protein... | Download Scientific Diagram
Tenascin-X (TenX) Ehlers-Danlos syndrome - EDS Wellness, Inc.
Tenascin-X Mediates Flow-Induced Suppression of EndMT and Atherosclerosis | Circulation Research
Rare neurological manifestations in a Saudi Arabian patient with Ehlers–Danlos syndrome and a novel homozygous variant in the TNXB gene - Al‐Harbi - 2022 - American Journal of Medical Genetics Part A -
