You are invited to apply for research funding from the Lowe Syndrome Trust.
The genetic basis for Lowe Syndrome is a defective gene OCRL1 that results in the deficiency of an enzyme Phosphatidylinositol 4,5-bisphosphate-5-phosphatase (OCRL1). Lowe’s oculocerebrorenal syndrome is a disorder affecting the brain, eyes, kidneys and bones.
New research funds are available for studies into genotype/phenotype correlations in Lowe Syndrome in the UK. Closing date of application is 13th June 2008.
For further information and application form please contact:
Lorraine Thomas, Lowe Syndrome Trust Telephone 0208 458 6791/ 0207 794 8858
lowetrust @ homechoice.co.uk
Please Email the details of the proposed research proposal using the word.doc form below.
Download the Lowe Syndrome Trust application form (word doc) click
here.