Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats. [electronic resource]

By: Contributor(s): Producer: 20060223Description: 222-4 p. digitalISSN:
  • 1087-0024
Subject(s): Online resources: In: The journal of investigative dermatology. Symposium proceedings vol. 10
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Publication Type: Journal Article; Research Support, N.I.H., Extramural

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