Cargando…
A novel apolipoprotein E mutation (p.Arg150Cys) in a Chinese patient with lipoprotein glomerulopathy
Autores principales: | Ku, Ming, Tao, Cai, Zhou, An-An, Cheng, Yuan, Wan, Qi-Jun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365261/ https://www.ncbi.nlm.nih.gov/pubmed/30614865 http://dx.doi.org/10.1097/CM9.0000000000000050 |
Ejemplares similares
-
A novel apolipoprotein E mutation, ApoE Ganzhou (Arg43Cys), in a Chinese son and his father with lipoprotein glomerulopathy: two case reports
por: Wang, Runxiu, et al.
Publicado: (2022) -
H Syndrome Presenting with Sinus of Valsalva Aneurysm and Possible Founder Mutation (p.Arg134cys) in Indian Patients
por: Amalnath, Deepak, et al.
Publicado: (2023) -
Lipoprotein Glomerulopathy Associated with a Mutation in Apolipoprotein E
por: Magistroni, Riccardo, et al.
Publicado: (2013) -
Apolipoprotein E ε4 Is Associated With the Development of Incident Dementia in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Patients With p.Arg544Cys Mutation
por: Lee, Jung Seok, et al.
Publicado: (2020) -
Identification of p.Arg205Cys in CASR in an autosomal dominant hypocalcaemia type 1 pedigree: A case report
por: Ji, Yubing, et al.
Publicado: (2021)