Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub‐Saharan Africa-Reference-Cited by-同舟云学术

Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub‐Saharan Africa

Published:2014-01-27 Issue:3 Volume:2 Page:254-260
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Butali Azeez¹,Mossey Peter A.²,Adeyemo Wasiu L.³,Eshete Mekonen A.⁴,Gaines LauRen A.¹,Even Dee¹,Braimah Ramat O.⁵,Aregbesola Babatunde S.⁵,Rigdon Jennifer V.¹,Emeka Christian I.³,James Olutayo³,Ogunlewe Mobolanle O.³,Ladeinde Akinola L.³,Abate Fikre⁴,Hailu Taye⁴,Mohammed Ibrahim⁴,Gravem Paul E.⁴,Deribew Milliard⁴,Gesses Mulualem⁴,Adeyemo Adebowale A.⁶,Murray Jeffrey C.¹

Affiliation:

1. Department of Oral Pathology Radiology and Medicine College of Dentistry University of Iowa Iowa City Iowa

2. Department of Orthodontics University of Dundee Dundee Scotland

3. College of Medicine University of Lagos Lagos Nigeria

4. Addis Ababa University Addis Ababa Ethiopia

5. Obafemi Awolowo University Ile‐Ife Nigeria

6. Center for Research on Genomics and Global Health National Human Genome Research Institute National Institutes of Health Bethesda Maryland

Funder

NIDCR

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.66

Reference20 articles.

1. A method and server for predicting damaging missense mutations

2. Novel IRF6 mutations in Honduran Van der Woude syndrome patients;Birkeland A. C.;Mol. Med. Rep.,2011

3. Replication of Genome Wide Association Identified Candidate Genes Confirm the Role of Common and Rare Variants inPAX7andVAX1in the Etiology of Nonsyndromic CL(P)

4. 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

5. IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign

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