Cargando…
Novel POLR1C mutation in RNA polymerase III‐related leukodystrophy with severe myoclonus and dystonia
INTRODUCTION: RNA polymerase III (Pol III)‐related leukodystrophies are a group of autosomal recessive neurodegenerative disorders caused by mutations in POLR3A and POLR3B. Recently a recessive mutation in POLR1C causative of Pol III‐related leukodystrophies was identified. METHODS: We report the ca...
Autores principales: | Kraoua, Ichraf, Karkar, Adnane, Drissi, Cyrine, Benrhouma, Hanene, Klaa, Hedia, Samaan, Simon, Renaldo, Florence, Elmaleh, Monique, Ben Hamouda, Mohamed, Abdelhak, Sonia, Boespflug‐Tanguy, Odile, Ben Youssef‐Turki, Ilfghem, Dorboz, Imen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732337/ https://www.ncbi.nlm.nih.gov/pubmed/31368241 http://dx.doi.org/10.1002/mgg3.914 |
Ejemplares similares
-
Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation
por: Dorboz, Imen, et al.
Publicado: (2018) -
Rasmussen's Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review
por: Klaa, Hedia, et al.
Publicado: (2020) -
Pediatric Multiple Sclerosis in Tunisia: A Retrospective Study over 11 Years
por: Ben Achour, Nedia, et al.
Publicado: (2017) -
Mirror Movements and Myelomeningocele: Report of A Single Case and Review of Literature
por: RéBAI, Ibtihel, et al.
Publicado: (2013) -
Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort
por: Douma, Bissene, et al.
Publicado: (2021)