A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene. [electronic resource]

By: Contributor(s): Producer: 20060203Description: 1072; author reply 1073 p. digitalISSN:
  • 0007-0963
Subject(s): Online resources: In: The British journal of dermatology vol. 153
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Publication Type: Comment; Letter

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