Cargando…
Clinical and Genetic Characterization of Female Dystrophinopathy
BACKGROUND AND PURPOSE: Duchenne and Becker muscular dystrophies are the most common X-linked recessive muscular dystrophies. Dystrophin gene mutations usually affect men, but reportedly 2.5-7.8% of women are affected and are classified as symptomatic carriers. The aim of this study was to clinicall...
Autores principales: | Lee, Seung Ha, Lee, Jung Hwan, Lee, Kyung-A, Choi, Young-Chul |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neurological Association
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507379/ https://www.ncbi.nlm.nih.gov/pubmed/26022459 http://dx.doi.org/10.3988/jcn.2015.11.3.248 |
Ejemplares similares
-
Clinical and genetic spectra in patients with dystrophinopathy in Korea: A single-center study
por: Yun, UnKyu, et al.
Publicado: (2021) -
Clinical and genetic characteristics of female dystrophinopathy carriers
por: Zhong, Jingzi, et al.
Publicado: (2019) -
MicroRNAs in Dystrophinopathy
por: Lee, Ahyoung, et al.
Publicado: (2022) -
Medical Attitudes Survey for Female Dystrophinopathy Carriers in Japan
por: Kobayashi, Michio, et al.
Publicado: (2018) -
The Expanding Spectrum of Dystrophinopathies: HyperCKemia to Manifest Female Carriers
por: Suthar, Renu, et al.
Publicado: (2021)