Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Original publication

DOI

10.1136/jme.27.3.148

Type

Journal article

Journal

J Med Ethics

Publication Date

06/2001

Volume

27

Pages

148 - 150

Keywords

Biomedical and Behavioral Research, Genetics and Reproduction, Adolescent, Clinical Trials as Topic, Ethics Committees, Fatal Outcome, Genetic Therapy, Human Experimentation, Humans, Informed Consent, Male, Ornithine Carbamoyltransferase Deficiency Disease, Patient Selection, Quality-Adjusted Life Years, Research Subjects