New Arab family with cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome suggests a possible founder effect for the c.223delG mutation
2015; Wiley; Volume: 42; Issue: 8 Linguagem: Inglês
10.1111/1346-8138.12917
ISSN1346-8138
AutoresSalma Ben‐Salem, Sobreira Nara, Aisha Al‐Shamsi, David Valle, Bassam R. Ali, Lihadh Al‐Gazali,
Tópico(s)Wnt/β-catenin signaling in development and cancer
ResumoThe Journal of DermatologyVolume 42, Issue 8 p. 821-822 Letter to the Editor New Arab family with cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome suggests a possible founder effect for the c.223delG mutation Salma Ben-Salem, Salma Ben-Salem Department of Pathology, College of Medicine and Heath Sciences, United Arab Emirates University, Al-Ain, United Arab EmiratesSearch for more papers by this authorSobreira Nara, Sobreira Nara Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USASearch for more papers by this authorAisha M. Al-Shamsi, Aisha M. Al-Shamsi Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab EmiratesSearch for more papers by this authorDavid Valle, David Valle Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USASearch for more papers by this authorBassam R. Ali, Bassam R. Ali Department of Pathology, College of Medicine and Heath Sciences, United Arab Emirates University, Al-Ain, United Arab EmiratesSearch for more papers by this authorLihadh Al-Gazali, Corresponding Author Lihadh Al-Gazali Department of Pediatrics, College of Medicine and Heath Sciences, United Arab Emirates University, Al-Ain, United Arab EmiratesCorrespondence: Lihadh Al-Gazali, F.R.C.P., Department of Pediatrics, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box 17666, Al-Ain, UAE. Email: l.algazali@uaeu.ac.aeSearch for more papers by this author Salma Ben-Salem, Salma Ben-Salem Department of Pathology, College of Medicine and Heath Sciences, United Arab Emirates University, Al-Ain, United Arab EmiratesSearch for more papers by this authorSobreira Nara, Sobreira Nara Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USASearch for more papers by this authorAisha M. Al-Shamsi, Aisha M. Al-Shamsi Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab EmiratesSearch for more papers by this authorDavid Valle, David Valle Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USASearch for more papers by this authorBassam R. Ali, Bassam R. Ali Department of Pathology, College of Medicine and Heath Sciences, United Arab Emirates University, Al-Ain, United Arab EmiratesSearch for more papers by this authorLihadh Al-Gazali, Corresponding Author Lihadh Al-Gazali Department of Pediatrics, College of Medicine and Heath Sciences, United Arab Emirates University, Al-Ain, United Arab EmiratesCorrespondence: Lihadh Al-Gazali, F.R.C.P., Department of Pediatrics, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box 17666, Al-Ain, UAE. Email: l.algazali@uaeu.ac.aeSearch for more papers by this author First published: 11 May 2015 https://doi.org/10.1111/1346-8138.12917Citations: 7Read 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 No abstract is available for this article.Citing Literature Volume42, Issue8August 2015Pages 821-822 RelatedInformation
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