Cargando…
Mixed Dubin-Gilbert Syndrome: A Compound Heterozygous Phenotype of Two Novel Variants in ABCC2 Gene
Autores principales: | Jiang, Jun, Wang, Hua-Gui, Wu, Wei-Li, Peng, Xiang-Xin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407029/ https://www.ncbi.nlm.nih.gov/pubmed/28397734 http://dx.doi.org/10.4103/0366-6999.204108 |
Ejemplares similares
-
Concurrence of novel mutations causing Gilbert’s and Dubin–Johnson syndrome with poor clinical outcomes in a Han Chinese family
por: Zhou, Tai-Cheng, et al.
Publicado: (2022) -
Case Report: Three novel pathogenic ABCC2 mutations identified in two patients with Dubin–Johnson syndrome
por: Zhao, Chenyu, et al.
Publicado: (2022) -
Genotype–Phenotype Association in ABCC2 Exon 18 Missense Mutation Leading to Dubin–Johnson Syndrome: A Case Report
por: Kim, Ji-Hoon, et al.
Publicado: (2022) -
Clinical characteristics and ABCC2 genotype in Dubin-Johnson syndrome: A case report and review of the literature
por: Wu, Huan, et al.
Publicado: (2021) -
Dubin's lives /
por: Malamud, Bernard