Novel Genetic, Clinical, and Pathomechanistic Insights into TFG-Associated Hereditary Spastic Paraplegia
HUMAN MUTATION
UKRI| Investigation of the molecular aspects of growth and development ,
UKRI| Accelerated Discovery of Molecules and Biological Pathways Perturbed in Mendelian Neurological Diseases
Authors: Gaurav V. Harlalka; Meriel E. McEntagart; Neerja Gupta; Anna E. Skrzypiec; Mariusz W. Mucha; Barry A. Chioza; Michael A. Simpson; +14 Authors
Gaurav V. Harlalka; Meriel E. McEntagart; Neerja Gupta; Anna E. Skrzypiec; Mariusz W. Mucha; Barry A. Chioza; Michael A. Simpson; Ajith Sreekantan-Nair; Anthony Pereira; Sven Günther; Amir Jahic; Hamid Modarres; Heather Moore-Barton; Richard C. Trembath; Madhulika Kabra; Emma L. Baple; Seema Thakur; Michael A. Patton; Christian Beetz; Robert Pawlak; Andrew H. Crosby;
doi: 10.1002/humu.23060
Novel Genetic, Clinical, and Pathomechanistic Insights into TFG-Associated Hereditary Spastic Paraplegia
Related Organizations
- University of Exeter United Kingdom
- Royal Devon University Healthcare NHS Foundation Trust United Kingdom
- All India Institute of Medical Sciences India
- Jena University Hospital Germany
- Guy's and St Thomas' NHS Foundation Trust United Kingdom
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citations
Citations provided by BIP!
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
popularity
Popularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
25
Top 10%
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