Evidence for Genetic Heterogeneity in Benign Familial Hematuria-Reference-Cited by-同舟云学术

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Evidence for Genetic Heterogeneity in Benign Familial Hematuria

Published:1999 Issue:4 Volume:19 Page:464-467
ISSN:0250-8095
Container-title:American Journal of Nephrology
language:en
Short-container-title:Am J Nephrol

Author:

Piccini Monica,Casari Giorgio,Zhou Janhua,Bruttini Mirella,Volti Salvatore Li,Ballabio Andrea,Renieri Alessandra

Publisher

S. Karger AG

Subject

Nephrology

Cited by 36 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. Morning Glory Syndrome associated with Autosomal Dominant Alport Syndrome with a Heterozygous COL4A4 Mutation;Childhood Kidney Diseases;2021-12-31

2. An update on current and potential genetic insights and diagnosis of Alport syndrome;Expert Opinion on Orphan Drugs;2020-06-02

3. Alport syndrome: facts and opinions;F1000Research;2017-01-17

4. A novel FN1 variant associated with familial hematuria: TBMN?;Clinical Biochemistry;2016-07

5. Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing;Journal of the American Society of Nephrology;2014-05-22

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