Novel V97G ASAH1 mutation found in Farber disease patients: unique appearance of the disease with an intermediate severity, and marked early involvement of central and peripheral nervous system. [electronic resource]

By: Contributor(s): Producer: 20120820Description: 400-4 p. digitalISSN:
  • 1872-7131
Subject(s): Online resources: In: Brain & development vol. 34
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Publication Type: Case Reports; Journal Article

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