[Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature]. [electronic resource]

By: Contributor(s): Producer: 19870626Description: 182-7 p. digitalISSN:
  • 0023-2165
Subject(s): Online resources: In: Klinische Monatsblatter fur Augenheilkunde vol. 190
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Publication Type: Case Reports; Journal Article

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