Cargando…
ADCY5-Related Dyskinesia: A Genetic Cause of Early-Onset Chorea-Report of Two Cases and a Novel Mutation
Autores principales: | Padmanabha, Hansashree, Ray, Somdattaa, Mahale, Rohan, Arunachal, Gautham, Singhi, Pratibha, Mailankody, Pooja, Pavagada, Mathuranath |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680907/ https://www.ncbi.nlm.nih.gov/pubmed/35002175 http://dx.doi.org/10.4103/aian.AIAN_1012_20 |
Ejemplares similares
-
DYT30 due to VPS16 Mutation: An Etiology of Childhood-Onset Generalized Dystonia
por: Shashi, Sridhar, et al.
Publicado: (2023) -
Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with TTC19 Gene Mutation
por: Mahale, Rohan R., et al.
Publicado: (2021) -
Childhood-Onset Generalized Dystonia Due to NDUFA9 Gene Mutation: An Expansion of Mutations Causing Leigh’s Syndrome
por: Singh, Raviprakash, et al.
Publicado: (2023) -
Rapidly Progressive Spastic Paraplegia Due to Hyperhomocysteinemia in Child with MTHFR Gene Mutation and Mitochondrial Complex I Deficiency: A Rare Association
por: Mahale, Rohan R., et al.
Publicado: (2021) -
Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence
por: Mahale, Rohan, et al.
Publicado: (2022)