Novel COL4A3 Mutations in African American Siblings With Autosomal Recessive Alport Syndrome-Reference-Cited by-同舟云学术

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Novel COL4A3 Mutations in African American Siblings With Autosomal Recessive Alport Syndrome

Published:2008-05 Issue:5 Volume:51 Page:e25-e28
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Cook Christine,Friedrich Christopher A.,Baliga Radhakrishna

Publisher

Elsevier BV

Subject

Nephrology

Reference14 articles.

1. Alport syndrome: Abnormalities of type IV collagen genes and proteins;Kashtan;Ren Fail,2000

2. Two previously unreported COL4A3 mutations in a patient with autosomal recessive Alport syndrome;Barnett,2005

3. Alport's syndrome in a Negro kindred;Schatz;Am J Ophthalmol,1971

Cited by 8 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. Systematic Review of Hearing Loss Genes in the African American Population;Otology & Neurotology;2019-06

2. A Novel Heterozygous Mutation of the COL4A3 Gene Causes a Peculiar Phenotype without Hematuria and Renal Function Impairment in a Chinese Family;Disease Markers;2019-02-10

3. Features of Autosomal Recessive Alport Syndrome: A Systematic Review;Journal of Clinical Medicine;2019-02-03

4. Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy;Pediatric Nephrology;2016-01-25

5. Targeted Exome Sequencing Integrated with Clinicopathological Information Reveals Novel and Rare Mutations in Atypical, Suspected and Unknown Cases of Alport Syndrome or Proteinuria;PLoS ONE;2013-10-10

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