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Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1111, doi. 10.1038/ng1870
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- Publication type:
- Article
Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation.
- Published in:
- 2005
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- Publication type:
- Letter
Autosomal Recessive Idiopathic Epilepsy in an Inbred Family from Turkey: Identification of a Putative Locus on Chromosome 9q32-33.
- Published in:
- Epilepsia (Series 4), 2004, v. 45, n. 5, p. 479, doi. 10.1111/j.0013-9580.2004.30903.x
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- Publication type:
- Article