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

Detalles Bibliográficos
Autores principales:	Bhusal, Mohan, Bhattarai, Sabina, Shah, Mahesh, Khadka, Anupa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2021
Materias:	Case Series
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022107/ https://www.ncbi.nlm.nih.gov/pubmed/33850991 http://dx.doi.org/10.1016/j.jdcr.2021.02.017

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