Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2047-9158
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia ; volume:8 ; number:1 ; day:26 ; month:6 ; year:2019 ; pages:1-13 ; date:12.2019
Translational neurodegeneration ; 8, Heft 1 (26.6.2019), 1-13, 12.2019
- Urheber
-
Wei, Qiao
Dong, Hai-Lin
Pan, Li-Ying
Chen, Cong-Xin
Yan, Yang-Tian
Wang, Rou-Min
Li, Hong-Fu
Liu, Zhi-Jun
Tao, Qing-Qing
Wu, Zhi-Ying
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s40035-019-0157-9
- URN
-
urn:nbn:de:101:1-2019092505325404148640
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 15.08.2025, 07:38 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Wei, Qiao
- Dong, Hai-Lin
- Pan, Li-Ying
- Chen, Cong-Xin
- Yan, Yang-Tian
- Wang, Rou-Min
- Li, Hong-Fu
- Liu, Zhi-Jun
- Tao, Qing-Qing
- Wu, Zhi-Ying
- SpringerLink (Online service)
Ähnliche Objekte (12)
Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
Hereditary spastic paraplegia from 1880 to 2017: an historical review
The role of inflammation in hereditary spastic paraplegia type 11
Non-pharmacological treatment of hereditary spastic paraplegia: a systematic review
Functional characterization of hereditary spastic paraplegia proteins spastin and ZFYVE27
AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant
Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia
Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
Hereditary spastic paraplegia from 1880 to 2017: an historical review
The role of inflammation in hereditary spastic paraplegia type 11
Non-pharmacological treatment of hereditary spastic paraplegia: a systematic review
Functional characterization of hereditary spastic paraplegia proteins spastin and ZFYVE27
AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant
Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia
Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
Hereditary spastic paraplegia from 1880 to 2017: an historical review
The role of inflammation in hereditary spastic paraplegia type 11
Non-pharmacological treatment of hereditary spastic paraplegia: a systematic review
Functional characterization of hereditary spastic paraplegia proteins spastin and ZFYVE27
AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant