Mutation analysis of novel candidate genes for X-linked Charcot Marie Tooth (CMTX3) neuropathy.

Funding Activity

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Funded Activity Summary

Our goal is to explore how peripheral nerves degenerate by identifying the gene mutation causing an X linked form of Charcot Marie Tooth neuropathy (CMTX3). Using bioinformatic resources and state of the art gene mutation scanning we will complete characterisation and systematic screening of candidate genes and novel transcripts in the region. Discovery of this gene will provide a means to determine mechanisms causing axonal degeneration and lead to targeted therapeutic treatment strategies.

Funded Activity Details

Start Date: 01-01-2008

End Date: 01-01-2009

Funding Scheme: NHMRC Project Grants

Funding Amount: $191,434.00

Funder: National Health and Medical Research Council

Research Topics

ANZSRC Field of Research (FoR)

Neurogenetics

ANZSRC Socio-Economic Objective (SEO)

There are no SEO codes available for this funding activity

Other Keywords

Axonal degeneration | Charcot-Marie-Tooth Disease | Inherited disorders | Inherited peripheral neuropathies | Molecular basis of disease | Mutation analysis | Neurodegeneration | Positional cloning