JAAD Case Reports (Apr 2021)

Congenital erythropoietic porphyria: A case series of a rare uroporphyrinogen III synthase gene mutation in Nepalese patients

  • Mohan Bhusal, MD,
  • Sabina Bhattarai, MD,
  • Mahesh Shah, MD,
  • Anupa Khadka, MBBS

Journal volume & issue
Vol. 10
pp. 102 – 106

Abstract

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No abstracts available.

Keywords