Mutation and Polymorphism Report

You have free access to this content

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

  1. M.E. Sáez1,
  2. A. Ruiz1,
  3. A. Cebrián2,
  4. F. Morales3,
  5. M. Robledo2,
  6. G. Antiñolo1,
  7. S. Borrego1

Article first published online: 27 DEC 1999

DOI: 10.1002/(SICI)1098-1004(200001)15:1<122::AID-HUMU41>3.0.CO;2-7

Issue

Human Mutation

Human Mutation

Special Issue: The HUGO Mutation Database Initiative: Issues, Databases, and Perspectives for the New Millennium

Volume 15, Issue 1, page 122, January 2000

Additional Information

How to Cite

Sáez, M.E., Ruiz, A., Cebrián, A., Morales, F., Robledo, M., Antiñolo, G. and Borrego, S. (2000), A new germline mutation, R600Q, within the coding region of RET proto-oncogene: A rare polymorphism or a MEN 2 causing mutation? . Hum. Mutat., 15: 122. doi: 10.1002/(SICI)1098-1004(200001)15:1<122::AID-HUMU41>3.0.CO;2-7

Author Information

  1. 1

    Unidad de Genética Médica y Diagnóstico Prenatal, Hospitales Universitarios Virgen del Rocío, Sevilla, Spain

  2. 2

    Departamento de Genética, Fundación Jímenez Díaz, Madrid, Spain

  3. 3

    Sección de Endocrinología, Hospital Universitario Infanta Cristina, Badajoz, Spain

  1. †

    Acknowledgments: This work was supported by grants 97/0339 and 98/0898 from the Fondo de Investigaciones Sanitarias (Spain).

Publication History

  1. Issue published online: 27 DEC 1999
  2. Article first published online: 27 DEC 1999
  3. Manuscript Accepted: 4 NOV 1999
  4. Manuscript Received: 14 JUL 1999

SEARCH

SEARCH BY CITATION

ARTICLE TOOLS

Get PDF (11K)

No abstract is available for this article.

Get PDF (11K)