Alport syndrome and diffuse leiomyomatosis: Deletions in the 5′ end of the COL4A5 collagen gene-Reference-Cited by-同舟云学术

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Alport syndrome and diffuse leiomyomatosis: Deletions in the 5′ end of the COL4A5 collagen gene

Published:1992-11 Issue:5 Volume:42 Page:1178-1183
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Antignac Corinne,Zhou Jing,Sanak Marek,Cochat Pierre,Roussel Bernard,Deschênes Georges,Gros Françoise,Knebelmann Bertrand,Hors-Cayla Marie-Claude,Tryggvason Karl,Gubler Marie-Claire

Publisher

Elsevier BV

Subject

Nephrology

Reference40 articles.

1. Hereditary familial congenital haemorrhagic nephritis;Alport;Brit Med J,1927

2. Alport syndrome;Atkin,1988

3. Alport's syndrome: A report of 58 cases and a review of the literature;Gubler;Am J Med,1981

4. The genetics of classic Alport's syndrome;Flinter;Lancet,1988

5. Mapping of Alport syndrome to the long arm of the X chromosome;Atkin;Am J Hum Genet,1988

Cited by 99 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. Alport syndrome with pelvic leiomyomatosis: The role of hormonal suppression;Journal of Case Reports and Images in Obstetrics and Gynecology;2022-09-19

2. Leiomyomatosis in an Infant With a SUFU Splice Site Variant: Case Report;Journal of Pediatric Hematology/Oncology;2022-04-04

3. Evolving role of patient registries in Alport syndrome;Future Rare Diseases;2021-06

4. Multidisciplinary Management of Alport Syndrome: Current Perspectives;Journal of Multidisciplinary Healthcare;2021-05

5. Uterine Mesenchymal Neoplasia;Practical Gynecologic Pathology;2021

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