Cargando…
Spastic Paraplegia Type 8: A First Report from India
Autores principales: | Mahale, Rohan, Arunachal, Gautam, Davuluri, Anudeep, Padmanabha, Hansashree, Mailankody, Pooja |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170995/ https://www.ncbi.nlm.nih.gov/pubmed/37179679 http://dx.doi.org/10.4103/aian.aian_901_22 |
Ejemplares similares
-
Hereditary Spastic Paraplegia due to LYST Gene Mutation: A Novel Causative Gene
por: Mahale, Rohan R., et al.
Publicado: (2023) -
Childhood-Onset Generalized Dystonia Due to NDUFA9 Gene Mutation: An Expansion of Mutations Causing Leigh’s Syndrome
por: Singh, Raviprakash, et al.
Publicado: (2023) -
Autoimmune Antibodies Positivity in Probable Sporadic Creutzfeldt–Jakob Disease: A Mini-Review of Literature
por: Anudeep, Davuluri Durga Srinivas, 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) -
Kennedy's Disease: A Second Genetically Confirmed Report from India
por: Shah, Rutul, et al.
Publicado: (2021)