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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author Bhusal, Mohan
Bhattarai, Sabina
Shah, Mahesh
Khadka, Anupa
author_facet Bhusal, Mohan
Bhattarai, Sabina
Shah, Mahesh
Khadka, Anupa
author_sort Bhusal, Mohan
collection PubMed
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spelling pubmed-80221072021-04-12 Congenital erythropoietic porphyria: A case series of a rare uroporphyrinogen III synthase gene mutation in Nepalese patients Bhusal, Mohan Bhattarai, Sabina Shah, Mahesh Khadka, Anupa JAAD Case Rep Case Series Elsevier 2021-02-25 /pmc/articles/PMC8022107/ /pubmed/33850991 http://dx.doi.org/10.1016/j.jdcr.2021.02.017 Text en © 2021 by the American Academy of Dermatology, Inc. Published by Elsevier, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Series
Bhusal, Mohan
Bhattarai, Sabina
Shah, Mahesh
Khadka, Anupa
Congenital erythropoietic porphyria: A case series of a rare uroporphyrinogen III synthase gene mutation in Nepalese patients
title Congenital erythropoietic porphyria: A case series of a rare uroporphyrinogen III synthase gene mutation in Nepalese patients
title_full Congenital erythropoietic porphyria: A case series of a rare uroporphyrinogen III synthase gene mutation in Nepalese patients
title_fullStr Congenital erythropoietic porphyria: A case series of a rare uroporphyrinogen III synthase gene mutation in Nepalese patients
title_full_unstemmed Congenital erythropoietic porphyria: A case series of a rare uroporphyrinogen III synthase gene mutation in Nepalese patients
title_short Congenital erythropoietic porphyria: A case series of a rare uroporphyrinogen III synthase gene mutation in Nepalese patients
title_sort congenital erythropoietic porphyria: a case series of a rare uroporphyrinogen iii synthase gene mutation in nepalese patients
topic Case Series
url 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
work_keys_str_mv AT bhusalmohan congenitalerythropoieticporphyriaacaseseriesofarareuroporphyrinogeniiisynthasegenemutationinnepalesepatients
AT bhattaraisabina congenitalerythropoieticporphyriaacaseseriesofarareuroporphyrinogeniiisynthasegenemutationinnepalesepatients
AT shahmahesh congenitalerythropoieticporphyriaacaseseriesofarareuroporphyrinogeniiisynthasegenemutationinnepalesepatients
AT khadkaanupa congenitalerythropoieticporphyriaacaseseriesofarareuroporphyrinogeniiisynthasegenemutationinnepalesepatients

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