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
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