Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module - ScienceDirect
Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant
Frontiers | Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome
Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia - Lao - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Tenascin XB Is a Novel Diagnostic Marker for Malignant Mesothelioma | Anticancer Research
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Missense mutations in TNXB as a cause of VUR. (A) Exons and protein... | Download Scientific Diagram
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population | Journal of Human Genetics
PDF) A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition | Nature Genetics
New TNXB Mutation in EDS Patient May Be Cause of Rare Lung Collapse
High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia - ScienceDirect
Tenascin-X (TenX) Ehlers-Danlos syndrome - EDS Wellness, Inc.
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 -
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Compound heterozygous mutations of the TNXB gene cause primary myopathy - ScienceDirect
Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients - Demirdas - 2017 - Clinical Genetics - Wiley Online Library
Tenascin-X Mediates Flow-Induced Suppression of EndMT and Atherosclerosis | Circulation Research
