Combination of a novel frameshift mutation (1929delCA) and a recurrent nonsense mutation (W610X) of the LAMB3 gene in a Japanese patient with Herlitz junctional epidermolysis bullosa, and their application for prenatal testing. [electronic resource]

By: Contributor(s): Producer: 19990104Description: 1239-41 p. digitalISSN:
  • 0022-202X
Subject(s): Online resources: In: The Journal of investigative dermatology vol. 111
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Publication Type: Letter; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

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