Novel mutations of IRF6 gene in Taiwanese Van der Woude syndrome patients-Reference-Cited by-同舟云学术

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Novel mutations of IRF6 gene in Taiwanese Van der Woude syndrome patients

Published:2019-04 Issue:2 Volume:60 Page:218-220
ISSN:1875-9572
Container-title:Pediatrics & Neonatology
language:en
Short-container-title:Pediatrics & Neonatology

Author:

Wang Tzu-Jou,Hsieh Kai-Shen,Lai Jui-Pin,Tsai Meng-Han,Liang Yi-Chih,Chang Yen-Hsun

Funder

Chang Gung Memorial Hospital

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference7 articles.

1. Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome;de Lima;Genet Med,2009

2. Van der Woude syndrome: a review. Cardinal signs, epidemiology, associated features, differential diagnosis, expressivity, genetic counselling and treatment;Rizos;Eur J Orthod,2004

3. Conserved transactivation domain shared by interferon regulatory factors and Smad morphogens;Eroshkin;J Mol Med (Berl),1999

4. Monozygotic twins with variable expression of Van der Woude syndrome;Jobling;Am J Med Genet A,2011

5. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes;Kondo;Nat Genet,2002

Cited by 5 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. A novel IRF6 gene mutation impacting the regulation of TGFβ2-AS1 in the TGFβ pathway: A mechanism in the development of Van der Woude syndrome;Frontiers in Genetics;2024-06-05

2. Causal Variations at IRF6 Gene Identified in Van der Woude Syndrome Pedigrees;The Cleft Palate Craniofacial Journal;2023-03-03

3. Identification of a Novel Variant of ARHGAP29 in a Chinese Family with Nonsyndromic Cleft Lip and Palate;BioMed Research International;2020-10-23

4. Non‐random distribution of deleterious mutations in the DNA and protein‐binding domains of IRF6 are associated with Van Der Woude syndrome;Molecular Genetics & Genomic Medicine;2020-06-17

5. Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome;Molecular Genetics & Genomic Medicine;2020-02-28

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