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

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

Bibliographic Details
Main Authors: Mohan Bhusal, MD, Sabina Bhattarai, MD, Mahesh Shah, MD, Anupa Khadka, MBBS
Format: Article
Language:English
Published: Elsevier 2021-04-01
Series:JAAD Case Reports
Subjects:
congenital erythropoietic porphyria
L139R mutation
Nepal
uroporphyrinogen III synthase
Online Access:http://www.sciencedirect.com/science/article/pii/S2352512621001351

Internet

http://www.sciencedirect.com/science/article/pii/S2352512621001351

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