Wyman Chen
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View article: Assessment of ataxia phenotype in a new mouse model of galactose‐1 phosphate uridylyltransferase (GALT) deficiency
Assessment of ataxia phenotype in a new mouse model of galactose‐1 phosphate uridylyltransferase (GALT) deficiency Open
Despite adequate dietary management, patients with classic galactosemia continue to have increased risks of cognitive deficits, speech dyspraxia, primary ovarian insufficiency, and abnormal motor development. A recent evaluation of a new g…