Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: Identification of the first large deletion in ASAH1 gene

Published 2013 View Full Article

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Title
Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: Identification of the first large deletion in ASAH1 gene
Authors
Keywords
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Journal
MOLECULAR GENETICS AND METABOLISM
Volume 109, Issue 3, Pages 276-281
Publisher
Elsevier BV
Online
2013-05-05
DOI
10.1016/j.ymgme.2013.04.019

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