Associated Papers
Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification.
Bloch-Zupan A et al.
Frontiers in Physiology, 2023
Novel LTBP3 mutations associated with thoracic aortic aneurysms and dissections.
Zhu G et al.
Orphanet Journal of Rare Diseases, 2021
Genotype-phenotype correlation and expansion of orodental anomalies in LTBP3-related disorders.
Intarak N et al.
Molecular Genetics and Genomics : Mgg, 2019
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.
Prasad MK et al.
Journal of Medical Genetics, 2016
26502894 (PubMed )
Supplement: jmedgenet-2015-103302-s1.pdf
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.
Huckert M et al.
Human Molecular Genetics, 2015
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