Vesicourethral reflux-induced renal failure in a patient with ICF syndrome due to a novelDNMT3Bmutation-Reference-Cited by-同舟云学术

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Vesicourethral reflux-induced renal failure in a patient with ICF syndrome due to a novelDNMT3Bmutation

Published:2016-09-08 Issue:12 Volume:170 Page:3253-3257
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kutluğ Seyhan¹,Ogur Gönül²,Yilmaz Aysegül²,Thijssen Peter E.³,Abur Ummet²,Yildiran Alisan¹

Affiliation:

1. Division of Immunology and Allergy; Department of Pediatrics; Faculty of Medicine; Ondokuz Mayıs University; Samsun Turkey

2. Department of Pediatric Genetics; Faculty of Medicine; Ondokuz Mayıs University; Samsun Turkey

3. Department of Human Genetics; Leiden University Medical Center; Leiden The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference17 articles.

1. Defective B-cell-negative selection and terminal differentiation in the ICF syndrome;Blanco-Betancourt;Blood,2004

2. Immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome, due to ZBTB24 mutations, presenting with large cerebral cyst;Cerbone;Am J Med Genet Part A,2012

3. Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2;De Greef;Am J Hum Genet,2011

4. Clinical spectrum of immunodeficiency, centromeric instability, and facial dysmorphism (ICF syndrome);Hagleitner;J Med Genet,2008

5. ICF syndrome in Saudi Arabia: Immunological, cytogenetic and molecular analysis;Kaya;J Clin Immunol,2011

Cited by 4 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. Evaluation of Clinical and Immunological Alterations Associated with ICF Syndrome;Journal of Clinical Immunology;2023-12-22

2. Epigenetic syndromes with immune deficiency;Stiehm's Immune Deficiencies;2020

3. The gene mutations and subtelomeric DNA methylation in immunodeficiency, centromeric instability and facial anomalies syndrome;Autoimmunity;2019-08-18

4. Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2;Clinical Genetics;2017-03-07

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