Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome – Video


Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome
Our results suggest that CWF19L1 mutations may be a novel cause of recessive ataxia with developmental delay. Our research may help with diagnosis, especially in Turkey, identify causes of...

By: Neurology Journal

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Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome - Video

Coast to Coast Irish Charity Cycle Fundraising to Cure Friedreich’s Ataxia Disease – Video


Coast to Coast Irish Charity Cycle Fundraising to Cure Friedreich #39;s Ataxia Disease
DONATE :http://www.OnYourBikeAtaxia.com A Fundraising Charity Cycle from the East to the West of Ireland over the June Bank Holiday Weekend 2015. Our Good Fr...

By: The Lads

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Coast to Coast Irish Charity Cycle Fundraising to Cure Friedreich's Ataxia Disease - Video