A new germline mutation, R600Q, within the coding region ofRET proto-oncogene: A rare polymorphism or a MEN 2 causing mutation?

Human MutationVolume 15, Issue 1 p. 122-122 Mutation and Polymorphism ReportFree Access A new germline mutation, R600Q, within the coding region of RET proto-oncogene: A rare polymorphism or a MEN 2 causing mutation? † M.E. Sáez, M.E. Sáez Unidad de Genética Médica y Diagnóstico Prenatal, Hospitales Universitarios Virgen del Rocío, Sevilla, SpainSearch for more papers by this authorA. Ruiz, A. Ruiz Unidad de Genética Médica y Diagnóstico Prenatal, Hospitales Universitarios Virgen del Rocío, Sevilla, SpainSearch for more papers by this authorA. Cebrián, A. Cebrián Departamento de Genética, Fundación Jímenez Díaz, Madrid, SpainSearch for more papers by this authorF. Morales, F. Morales Sección de Endocrinología, Hospital Universitario Infanta Cristina, Badajoz, SpainSearch for more papers by this authorM. Robledo, M. Robledo Departamento de Genética, Fundación Jímenez Díaz, Madrid, SpainSearch for more papers by this authorG. Antiñolo, G. Antiñolo Unidad de Genética Médica y Diagnóstico Prenatal, Hospitales Universitarios Virgen del Rocío, Sevilla, SpainSearch for more papers by this authorS. Borrego, S. Borrego Unidad de Genética Médica y Diagnóstico Prenatal, Hospitales Universitarios Virgen del Rocío, Sevilla, SpainSearch for more papers by this author M.E. Sáez, M.E. Sáez Unidad de Genética Médica y Diagnóstico Prenatal, Hospitales Universitarios Virgen del Rocío, Sevilla, SpainSearch for more papers by this authorA. Ruiz, A. Ruiz Unidad de Genética Médica y Diagnóstico Prenatal, Hospitales Universitarios Virgen del Rocío, Sevilla, SpainSearch for more papers by this authorA. Cebrián, A. Cebrián Departamento de Genética, Fundación Jímenez Díaz, Madrid, SpainSearch for more papers by this authorF. Morales, F. Morales Sección de Endocrinología, Hospital Universitario Infanta Cristina, Badajoz, SpainSearch for more papers by this authorM. Robledo, M. Robledo Departamento de Genética, Fundación Jímenez Díaz, Madrid, SpainSearch for more papers by this authorG. Antiñolo, G. Antiñolo Unidad de Genética Médica y Diagnóstico Prenatal, Hospitales Universitarios Virgen del Rocío, Sevilla, SpainSearch for more papers by this authorS. Borrego, S. Borrego Unidad de Genética Médica y Diagnóstico Prenatal, Hospitales Universitarios Virgen del Rocío, Sevilla, SpainSearch for more papers by this author First published: 27 December 1999 https://doi.org/10.1002/(SICI)1098-1004(200001)15:1<122::AID-HUMU41>3.0.CO;2-7Citations: 8 † Communicated by: Daniel F. Schorderet ‡ Online Citation: Human Mutation, Mutation and Polymorphism Report #94 (1999) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr94.pdf § Acknowledgments: This work was supported by grants 97/0339 and 98/0898 from the Fondo de Investigaciones Sanitarias (Spain). AboutPDF 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 No abstract is available for this article.Citing Literature Volume15, Issue1Special Issue: The HUGO Mutation Database Initiative: Issues, Databases, and Perspectives for the New MillenniumJanuary 2000Pages 122-122 RelatedInformation