The Hereditary Ataxias
Author:
Publisher
Elsevier
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4. Mutations in SLC6A19, Encoding B0AT1, Cause Hartnup Disorder;Kleta;Nat Genet,2004
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1. The histone deacetylase HDAC3 is essential for Purkinje cell function, potentially complicating the use of HDAC inhibitors in SCA1;Human Molecular Genetics;2014-03-04
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