Efficient detection of frequent eIF2B mutations for the rapid molecular diagnosis of CACH/VWM syndrome. [electronic resource]

By: Contributor(s): Producer: 20160913Description: 1317-23 p. digitalISSN:
  • 1873-2933
Subject(s): Online resources: In: Clinical biochemistry vol. 48
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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