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Aims of
A3243G
- To gather, collate and disseminate information relating to the A3243G point
mutation of the Mitochondrial DNA, suitable for a wide range of audiences
including Patients, Physicians, Researchers and the Media.
- To promote knowledge and understanding of the issues arising from this
Mitochondrial DNA point mutation in the Diabetic and Hearing Impaired
communities – from both a patient and health care management perspective.
- To provide a global support group for sufferers and their families.
- To keep all information on the web site up to date and pertinent.
- To become self financing, using a variety of means.
This will be achieved by:
- Encouraging
visitors to register at the website, and to complete an online survey.
- Generating
a copyrighted Newsletter on a regular basis.
- Generating
a variety of copyrighted documents about relevant topics, suitable for a
variety of audiences.
- Recruiting medically qualified
“Editors” to validate content.
- Providing
a repository of Published articles, (within the constraints of copyright,
e.g. links to PubMed abstracts).
- Creating
reciprocal links between relevant web sites.
- Adhering to a variety of protocols for online content, including ICRA and
HonCode(applied for).
Andy Collinson
Date Page Updated:
25 April 2005
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