Increased microvascular disease in X-linked and autosomal recessive Alport syndrome: a case control cross sectional observational study-Reference-Cited by-同舟云学术

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Increased microvascular disease in X-linked and autosomal recessive Alport syndrome: a case control cross sectional observational study

Published:2019-03-04 Issue:2 Volume:40 Page:129-134
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Smith James D.¹,Colville Deb¹,Lyttle Nicolette¹,Lamoureux Ecosse²³⁴,Savige Judy¹

Affiliation:

1. Department of Medicine, Royal Melbourne Hospital, The University of Melbourne, Parkville, Australia

2. Singapore Eye Research Institute, Yong Loo Lin School of Medicine, National University of Singapore, Singapore

3. Department of Ophthalmology, Centre for Eye Research Australia, The University of Melbourne, Melbourne, Australia

4. Duke-NUS Graduate Medical School, National University of Singapore, Singapore

Publisher

Informa UK Limited

Subject

Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2019.1589528

Reference42 articles.

1. Expert Guidelines for the Management of Alport Syndrome and Thin Basement Membrane Nephropathy

2. Genetic heterogeneity of Alport syndrome

3. Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

4. Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome

5. Alport's Syndrome, Goodpasture's Syndrome, and Type IV Collagen

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Heterozygous Pathogenic COL4A3 and COL4A4 Variants (Autosomal Dominant Alport Syndrome) Are Common, and Not Typically Associated With End-Stage Kidney Failure, Hearing Loss, or Ocular Abnormalities;Kidney International Reports;2022-09

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