Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia
2013; Wiley; Volume: 86; Issue: 5 Linguagem: Inglês
10.1111/cge.12312
ISSN1399-0004
AutoresSalma M. Wakil, Dorota Monies, Khushnooda Ramzan, S. Hagos, Lailá Bastaki, Brian F. Meyer, Saeed Bohlega,
Tópico(s)Neurogenetic and Muscular Disorders Research
ResumoClinical GeneticsVolume 86, Issue 5 p. 500-501 LETTER TO THE EDITOR Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia S.M. Wakil, Corresponding Author S.M. Wakil Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia Correspondence: Salma M. Wakil Department of Genetics King Faisal Specialist Hospital and Research Centre Riyadh Saudi Arabia Tel.: +966114647272×36485 Fax: +96614424585 e-mail: smajid@kfshrc.edu.sa; salmaw@yahoo.comSearch for more papers by this authorD.M. Monies, D.M. Monies Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this authorK. Ramzan, K. Ramzan Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this authorS. Hagos, S. Hagos Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this authorL. Bastaki, L. Bastaki Department of Clinical Genetics, Kuwait Medical Genetics Centre, KuwaitSearch for more papers by this authorB.F. Meyer, B.F. Meyer Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this authorS. Bohlega, S. Bohlega Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this author S.M. Wakil, Corresponding Author S.M. Wakil Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia Correspondence: Salma M. Wakil Department of Genetics King Faisal Specialist Hospital and Research Centre Riyadh Saudi Arabia Tel.: +966114647272×36485 Fax: +96614424585 e-mail: smajid@kfshrc.edu.sa; salmaw@yahoo.comSearch for more papers by this authorD.M. Monies, D.M. Monies Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this authorK. Ramzan, K. Ramzan Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this authorS. Hagos, S. Hagos Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this authorL. Bastaki, L. Bastaki Department of Clinical Genetics, Kuwait Medical Genetics Centre, KuwaitSearch for more papers by this authorB.F. Meyer, B.F. Meyer Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this authorS. Bohlega, S. Bohlega Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSearch for more papers by this author First published: 27 November 2013 https://doi.org/10.1111/cge.12312Citations: 26Read 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 Volume86, Issue5Special Issue: Genetics and Translational MedicineNovember 2014Pages 500-501 RelatedInformation
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