JAAD Case Reports (Jan 2022)

A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family

  • Sara Aldokhayel, MD,
  • Alballa Nouf, MD,
  • Aleedan Khalid, MD,
  • Alsaif Faisal, MD,
  • Alotaibi Maram, MD,
  • Alhumidi Ahmed, MD,
  • Alsaif Fahad, MD

Journal volume & issue
Vol. 19
pp. 97 – 99

Abstract

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No abstracts available.

Keywords