Correlation between FBN1 mutations and ocular features with ectopia lentis in the setting of Marfan syndrome and related fibrillinopathies-Reference-Cited by-同舟云学术

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Correlation between FBN1 mutations and ocular features with ectopia lentis in the setting of Marfan syndrome and related fibrillinopathies

Published:2021-09-28 Issue:12 Volume:42 Page:1637-1647
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Chen Ze‐Xu¹²³^ORCID,Chen Tian‐Hui¹²³,Zhang Min¹²³,Chen Jia‐Hui¹²³,Lan Li‐Na¹²³,Deng Michael¹²³,Zheng Jia‐Lei¹²³,Jiang Yong‐Xiang¹²³^ORCID

Affiliation:

1. Eye Institute and Department of Ophthalmology, Eye & ENT Hospital Fudan University Shanghai China

2. NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia Chinese Academy of Medical Sciences Shanghai China

3. Shanghai Key Laboratory of Visual Impairment and Restoration Shanghai China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24283

Reference43 articles.

1. Ectopia Lentis with Microspherophakia in Marfan Syndrome Resolved with Mydriasis

2. Prevalence of ectopia lentis and retinal detachment in Marfan syndrome

3. Fibrillin-1 regulates the bioavailability of TGFβ1

4. Analysis of Axial Length in Young Patients with Marfan Syndrome and Bilateral Ectopia Lentis by Z-Scores

5. Ocular findings in 87 adults with Ghent‐1 verified Marfan syndrome

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1. Genotype Associated With Visual Prognosis in Patients With Congenital Ectopia Lentis Following Lens Surgery: A Prospective Cohort Study;American Journal of Ophthalmology;2024-12

2. In Search of Mouse Models for Exfoliation Syndrome;American Journal of Ophthalmology;2024-11

3. Genotype-phenotype profile of global ASPH-associated ectopia lentis and clinical findings from a Chinese cohort;Gene;2024-10

4. Genotype-phenotype Correlations of Ocular Posterior Segment Abnormalities in Marfan Syndrome;Ophthalmology Science;2024-09

5. Mutations in ADAMTSL4 cause a unique form of autosomal-recessive congenital ectopia lentis;Experimental Eye Research;2024-09

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