Human and mouse disorders of pigmentation

Richard A. Spritz, Pei Wen Chiang, Naoki Oiso, Asem Alkhateeb

Research output: Contribution to journalReview article

59 Scopus citations

Abstract

Disorders of pigmentation were among the first genetic diseases ever recognized because of their visually striking clinical phenotypes, resulting from defects of pigmentary melanocytes. Recent years have seen remarkable progress in understanding these diseases, largely as a result of the systematic parallel study of human patients and inbred mice with similar phenotypes. Our understanding of disorders of pigmentation indicates that these diseases may be most usefully considered as abnormalities of melanocyte development, function, or survival.

Original languageEnglish (US)
Pages (from-to)284-289
Number of pages6
JournalCurrent Opinion in Genetics and Development
Volume13
Issue number3
DOIs
StatePublished - Jun 2003

ASJC Scopus subject areas

  • Genetics
  • Developmental Biology

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