Neurogenetics update

This publication has 11 references indexed in Scilit:

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• Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q
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• Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia
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• Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
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