TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Frontiers | Tenascin-X—Discovery and Early Research
Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module - ScienceDirect
Genes | Free Full-Text | Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population | Journal of Human Genetics
Frontiers | Genes and Pseudogenes: Complexity of the RCCX Locus and Disease
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Missense mutations in TNXB as a cause of VUR. (A) Exons and protein... | Download Scientific Diagram
Frontiers | Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant
Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients - Demirdas - 2017 - Clinical Genetics - Wiley Online Library
Differentially methylated region identified within tenascin X (TNXB).... | Download Scientific Diagram
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
PDF) A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia
Schematic diagram of CYP21A1P/CYP21A2 and TNXA/TNXB chimera genes. (A)... | Download Scientific Diagram
Tenascin-X, Congenital Adrenal Hyperplasia, and the CAH-X Syndrome | Semantic Scholar
Tenascin XB Is a Novel Diagnostic Marker for Malignant Mesothelioma | Anticancer Research
Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
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 -
Schematic diagram of CYP21A1P/CYP21A2 and TNXA/TNXB chimera genes. (A)... | Download Scientific Diagram
Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome
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
Frontiers | Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome
Compound heterozygous mutations of the TNXB gene cause primary myopathy - ScienceDirect
What is tenascin x (TNXB)? This might be the gene I am asked about the most. Many people wonder if their EDS could be caused by TNXB, and… | Instagram
