Absence of NOTCH2 and Hey2 mutations in a familial Alagille syndrome case with a novel frameshift mutation in JAG1

Abstract

American Journal of Medical Genetics Part AVolume 146A, Issue 7 p. 937-939 Research Letter Absence of NOTCH2 and Hey2 mutations in a familial Alagille syndrome case with a novel frameshift mutation in JAG1† Inaam El-Rassy, Inaam El-Rassy Department of Biochemistry, American University of Beirut (AUB), Beirut, LebanonSearch for more papers by this authorJad Bou-Abdallah, Jad Bou-Abdallah Department of Biochemistry, American University of Beirut (AUB), Beirut, LebanonSearch for more papers by this authorSara Al-Ghadban, Sara Al-Ghadban Department of Biochemistry, American University of Beirut (AUB), Beirut, LebanonSearch for more papers by this authorFadi Bitar, Fadi Bitar Department of Biochemistry, American University of Beirut (AUB), Beirut, Lebanon Department of Pediatrics, American University of Beirut (AUB), Beirut, LebanonSearch for more papers by this authorGeorges Nemer, Corresponding Author Georges Nemer gn08@aub.edu.lb Department of Biochemistry, American University of Beirut (AUB), Beirut, LebanonAmerican University of Beirut, Bliss Street, P.O. Box 110236, Beirut, Lebanon.Search for more papers by this author Inaam El-Rassy, Inaam El-Rassy Department of Biochemistry, American University of Beirut (AUB), Beirut, LebanonSearch for more papers by this authorJad Bou-Abdallah, Jad Bou-Abdallah Department of Biochemistry, American University of Beirut (AUB), Beirut, LebanonSearch for more papers by this authorSara Al-Ghadban, Sara Al-Ghadban Department of Biochemistry, American University of Beirut (AUB), Beirut, LebanonSearch for more papers by this authorFadi Bitar, Fadi Bitar Department of Biochemistry, American University of Beirut (AUB), Beirut, Lebanon Department of Pediatrics, American University of Beirut (AUB), Beirut, LebanonSearch for more papers by this authorGeorges Nemer, Corresponding Author Georges Nemer gn08@aub.edu.lb Department of Biochemistry, American University of Beirut (AUB), Beirut, LebanonAmerican University of Beirut, Bliss Street, P.O. Box 110236, Beirut, Lebanon.Search for more papers by this author First published: 11 February 2008 https://doi.org/10.1002/ajmg.a.32225Citations: 3 † How to cite this article: El-Rassy I, Bou-Abdallah J, Al-Ghadban S, Bitar F, Nemer G. 2008. Absence of NOTCH2 and Hey2 mutations in a familial Alagille syndrome case with a novel frameshift mutation in JAG1. Am J Med Genet Part A 146A:937–939. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume146A, Issue71 April 2008Pages 937-939 RelatedInformation