Cargando…
Mutations in HPCA Cause Autosomal-Recessive Primary Isolated Dystonia
Reports of primary isolated dystonia inherited in an autosomal-recessive (AR) manner, often lumped together as “DYT2 dystonia,” have appeared in the scientific literature for several decades, but no genetic cause has been identified to date. Using a combination of homozygosity mapping and whole-exom...
Autores principales: | Charlesworth, Gavin, Angelova, Plamena R., Bartolomé-Robledo, Fernando, Ryten, Mina, Trabzuni, Daniah, Stamelou, Maria, Abramov, Andrey Y., Bhatia, Kailash P., Wood, Nicholas W. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385177/ https://www.ncbi.nlm.nih.gov/pubmed/25799108 http://dx.doi.org/10.1016/j.ajhg.2015.02.007 |
Ejemplares similares
-
Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel
por: Mok, Kin Y, et al.
Publicado: (2014) -
Childhood‐Onset Choreo‐Dystonia Due to a Recurrent Novel Homozygous Nonsense
HPCA
Variant: Case Series and Literature Review
por: Magrinelli, Francesca, et al.
Publicado: (2022) -
The genetics of dystonia: new twists in an old tale
por: Charlesworth, Gavin, et al.
Publicado: (2013) -
Mutations in the Autoregulatory Domain of β-Tubulin 4a Cause Hereditary Dystonia
por: Hersheson, Joshua, et al.
Publicado: (2013) -
Autosomal recessive inheritance of ADCY5-related generalized dystonia and myoclonus
por: Barrett, Matthew J., et al.
Publicado: (2017)