Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome
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Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome
Burns R, Majczenko K, Xu J, Peng W, Yapici Z, Dowling JJ, Li JZ, Burmeister M. Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome. Neurology. 2014 Oct 31. pii: 10.1212/WNL.0000000000001053. [Epub ahead of print]
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