Ataxia and dysarthria due to an ABCA2 variant: Extension of the phenotypic spectrum
Author:
Funder
Higher Education Commission, Pakistan
Publisher
Elsevier BV
Subject
Clinical Neurology,Geriatrics and Gerontology,Neurology
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5. Complete coding sequence, promoter region, and genomic structure of the human ABCA2 gene and evidence for sterol-dependent regulation in macrophages;Kaminski;Biochem. Biophys. Res. Commun.,2001
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