latent transforming growth factor-beta-binding protein-2 [human, fibro - Nucleotide

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Autosomal Dominant Weill-Marchesani-Like Syndrome in a Chinese Family due to Novel Haplotypic Mutations in LTBP2. [Ophthalmic Res. 2024]
Autosomal Dominant Weill-Marchesani-Like Syndrome in a Chinese Family due to Novel Haplotypic Mutations in LTBP2.
Chen J, Wan J, Jin J, Jin G, Zheng Y, Zheng D, Zhong L. Ophthalmic Res. 2024; 67(1):340-347. Epub 2024 May 21.
Identification and phenotypic analysis of novel LTBP2 mutations in a Chinese cohort with congenital ectopia lentis. [Mol Vis. 2023]
Identification and phenotypic analysis of novel LTBP2 mutations in a Chinese cohort with congenital ectopia lentis.
Liu L, Guo D, Yang F, Qi H, Zhou Y, Zheng D, Jin G. Mol Vis. 2023; 29:169-179. Epub 2023 Oct 10.
Plasma LTBP2 as a potential biomarker in differential diagnosis of connective tissue disease-associated interstitial lung disease and idiopathic pulmonary fibrosis: a pilot study. [Clin Exp Med. 2023]
Plasma LTBP2 as a potential biomarker in differential diagnosis of connective tissue disease-associated interstitial lung disease and idiopathic pulmonary fibrosis: a pilot study.
Zou M, Hu X, Song W, Gao H, Wu C, Zheng W, Cheng Z. Clin Exp Med. 2023 Dec; 23(8):4809-4816. Epub 2023 Oct 21.

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Nucleotide