Associated Papers
Expanding the Clinical and Molecular Spectrum of TUBB2B Through Distinct Variants Identified Across Multiple Families.
Beheshti ST et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
The p.Ile202Thr Substitution in TUBB2B Can Be Associated with Syndromic Presentation of Congenital Fibrosis of the Extraocular Muscles.
Mancini C et al.
Genes, 2025
Insights on the Role of α- and β-Tubulin Isotypes in Early Brain Development.
Tantry MSA et al.
Molecular Neurobiology, 2023
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability.
Breuss MW et al.
Human Molecular Genetics, 2017
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