Generation of a human iPSC line from a patient with Leber congenital amaurosis caused by mutation in AIPL1. [electronic resource]

By: Contributor(s): Producer: 20190730Description: 151-155 p. digitalISSN:
  • 1876-7753
Subject(s): Online resources: In: Stem cell research vol. 33
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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