Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families. [electronic resource]

By: Contributor(s): Producer: 20170616Description: 1430-5 p. digitalISSN:
  • 1476-5438
Subject(s): Online resources: In: European journal of human genetics : EJHG vol. 24
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Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.

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