Rare Diseases Clinical Research Network (RDCRN),
Investigating the Effects of SPTSSA Variants on Sphingolipid Synthesis and Hereditary Spastic…
SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia
Overview of attention for article published in Brain, January 2023
Altmetric Badge
About this Attention Score
-
In the top 5% of all research outputs scored by Altmetric
-
High Attention Score compared to outputs of the same age (95th percentile)
-
Good Attention Score compared to outputs of the same age and source (75th percentile)
Readers on
- mendeley
- 33 Mendeley