12
Views
1
CrossRef citations to date
0
Altmetric
Original Article

New Molecular Genetic Defects Causing 11β-Hydroxylase Deficiency (CAH)

, , &
Pages 781-782 | Published online: 07 Jul 2009

References

  • Merke D. P., Tajima T., Chhabra A., Barnes K., Mancilla E., Baron J., Cutler J. RGB. J Clin Endocrinol Metab 1998; 83: 270–273
  • Peters J., Hampf M., Peters B., Bernhardt R. Molekularbiologie, Klinik und Therapie steroidbedingter Hypertonien. Handbuch der Molekularen Medizin, D. Ganten, K. Ruckpaul. Springer-Verlag Berlin Heidelberg, New York 1998; 413–452
  • Lifton R. P., Dluhy R. G., Powers M., Rich G. M., Cook S., Ulick S., Lalouel J. M. Nature 1992; 355: 262–265
  • Pascoe L., Curnow K., Slutsker L., Connell JMC, Speiser P., New M. I., White P. C. Proc Natl Acad Sci 1992; 89: 8327–8331

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.