Cargando…

Correction to: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia

Detalles Bibliográficos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2022
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586539/ https://www.ncbi.nlm.nih.gov/pubmed/36076346 http://dx.doi.org/10.1093/brain/awac254

Ejemplares similares

TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia
por: Tábara, Luis Carlos, et al.
Publicado: (2022)

Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia
por: Iqbal, Zafar, et al.
Publicado: (2017)

Rescue axonal defects by targeting mitochondrial dynamics in hereditary spastic paraplegias
por: Mou, Yongchao, et al.
Publicado: (2019)

ER Morphology in the Pathogenesis of Hereditary Spastic Paraplegia
por: Sonda, Sonia, et al.
Publicado: (2021)

A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutations
por: Abrahamsen, Greger, et al.
Publicado: (2015)

Correction to: Potential markers for sample size estimations in hereditary spastic paraplegia type 5
por: Lin, Qianqian, et al.
Publicado: (2021)

Correction to: Store-operated calcium entry is reduced in spastin-linked hereditary spastic paraplegia
Publicado: (2023)

Characterization of kinesin switch I mutations that cause hereditary spastic paraplegia
por: Jennings, Scott, et al.
Publicado: (2017)

Hereditary Spastic Paraplegia: An Update
por: Meyyazhagan, Arun, et al.
Publicado: (2022)

Current Knowledge of Endolysosomal and Autophagy Defects in Hereditary Spastic Paraplegia
por: Toupenet Marchesi, Liriopé, et al.
Publicado: (2021)

Lipids in the Physiopathology of Hereditary Spastic Paraplegias
por: Darios, Frédéric, et al.
Publicado: (2020)

Movement disorders in hereditary spastic paraplegias
por: Pedroso, Jose Luiz, et al.
Publicado: (2023)

Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
por: Chen, Xueping, et al.
Publicado: (2020)

A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76
por: Chinta, Vijayendra R., et al.
Publicado: (2022)

Hereditary spastic paraplegia with thin corpus callosum
por: Raina, Sujeet, et al.
Publicado: (2009)

Lysosome Function and Dysfunction in Hereditary Spastic Paraplegias
por: Edmison, Daisy, et al.
Publicado: (2021)

Lipid Droplets in the Pathogenesis of Hereditary Spastic Paraplegia
por: Tadepalle, Nimesha, et al.
Publicado: (2021)

Dysarthria in hereditary spastic paraplegia type 4
por: Jacinto-Scudeiro, Lais Alves, et al.
Publicado: (2022)

Defects in ER–endosome contacts impact lysosome function in hereditary spastic paraplegia
por: Allison, Rachel, et al.
Publicado: (2017)

Single cell morphology distinguishes genotype and drug effect in Hereditary Spastic Paraplegia
por: Wali, Gautam, et al.
Publicado: (2021)

Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!
por: Roubertie, Agathe, et al.
Publicado: (2019)

SPG20 mutation in three siblings with familial hereditary spastic paraplegia
por: Dardour, Leila, et al.
Publicado: (2017)

Genetic mutation analysis of hereditary spastic paraplegia: A retrospective study
por: Cui, Fang, et al.
Publicado: (2020)

CAPN1 Variants as Cause of Hereditary Spastic Paraplegia Type 76
por: Garcia-Berlanga, Jesus Eduardo, et al.
Publicado: (2019)

A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia
por: Helbig, Katherine L., et al.
Publicado: (2016)

Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia
por: Vaz, Frédéric M, et al.
Publicado: (2019)

Genetic and phenotypic characterization of complex hereditary spastic paraplegia
por: Kara, Eleanna, et al.
Publicado: (2016)

Clinical and genetic study of hereditary spastic paraplegia in Canada
por: Chrestian, Nicolas, et al.
Publicado: (2016)

Clinical Trial Designs and Measures in Hereditary Spastic Paraplegias
por: Trummer, Brian, et al.
Publicado: (2018)

Clinico-Investigative Profile of Hereditary Spastic Paraplegia in Children
por: Kamate, Mahesh, et al.
Publicado: (2019)

Pure or Complex Hereditary Spastic Paraplegia Type 4?
por: Finsterer, Josef
Publicado: (2019)

Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia
por: Saputra, Lydia, et al.
Publicado: (2021)

Hereditary spastic paraplegia initially diagnosed as cerebral palsy
por: Suchowersky, Oksana, et al.
Publicado: (2021)

The Puzzle of Hereditary Spastic Paraplegia: From Epidemiology to Treatment
por: Meyyazhagan, Arun, et al.
Publicado: (2022)

Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
por: Regensburger, Martin, et al.
Publicado: (2022)

Presynaptic endoplasmic reticulum architecture and hereditary spastic paraplegia
por: Pérez-Moreno, Juan José
Publicado: (2023)

ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia
por: Bouwkamp, Christian G., et al.
Publicado: (2018)

De novo REEP2 missense mutation in pure hereditary spastic paraplegia
por: Roda, Ricardo H., et al.
Publicado: (2017)

Screening for REEP1 Mutations in 31 Chinese Hereditary Spastic Paraplegia Families
por: Ma, Xinran, et al.
Publicado: (2020)

Association of an insertion mutation in PRRT2 with hereditary spastic paraplegia accompanied by polyneuropathy
por: Wang, Zhaoyu, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_1ppjbk1eshc4irc4js83908t48