ARV1 p.Gln62Ter, a novel mutation linked to developmental and epileptic encephalopathy-38
Abstract Developmental and epileptic encephalopathy is a rare and severe form of inherited neurodegenerative disorder characterized by various forms of seizures. This condition typically manifests between 4 and 7 months. Recent investigations have established a correlation between mutations in the A...
Saved in:
Main Authors: | Mostafa Neissi, Ayoob Radhi Al-Zaalan, Misagh Mohammadi-Asl, Mojdeh Roghani, Javad Mohammadi-Asl, Kamele Jorfi |
---|---|
Format: | Article |
Language: | English |
Published: |
Springer
2025-02-01
|
Series: | Journal of Rare Diseases |
Subjects: | |
Online Access: | https://doi.org/10.1007/s44162-025-00066-1 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The Relationship between Depression, Doing Exercise, Age and Cigarettes Smoking in ARV - HIV Patients
by: Vu Hoang Anh Nguyen, et al.
Published: (2024-07-01) -
Integrated analysis of proteomics and metabolomics in infantile epileptic spasms syndrome
by: Jun Chen, et al.
Published: (2025-02-01) -
Treatment efficacy for infantile epileptic spasms syndrome in children with trisomy 21
by: Henry Chen, et al.
Published: (2025-02-01) -
Genetics and biological characteristics of duck reoviruses isolated from ducks and geese in China
by: Xiaohong Sun, et al.
Published: (2025-02-01) -
Monoclonal anti-CD38 therapy in human myeloma: retrospects and prospects
by: Alberto L. Horenstein, et al.
Published: (2025-02-01)