Systemic Lupus Erythematosus and Hereditary Coproporphyria: Two Different Entities Diagnosed by WES in the Same Patient

BACKGROUND: Hereditary coproporphyria (HCP) is a rare autosomal dominant disorder caused by a partial deficiency of coproporphyrinogen III oxidase (CPOX), and systemic lupus erythematosus (SLE) is an autoimmune disease with a strong genetic predisposition. SLC7A7 (solute carrier family 7 member 7) m...

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Detalles Bibliográficos
Autores principales: Liu, Anlei, Zhou, Lingli, Zhu, Huadong, Li, Yi, Yang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167117/
https://www.ncbi.nlm.nih.gov/pubmed/35669728
http://dx.doi.org/10.1155/2022/9096999

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167117/
https://www.ncbi.nlm.nih.gov/pubmed/35669728
http://dx.doi.org/10.1155/2022/9096999

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