Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia
Work
Year: 2022
Type: article
Source: Genetics in Medicine
Institutions University College London, National Hospital for Neurology and Neurosurgery, Alexandria University, Inserm, Université de Montpellier +32 more
Cites: 23
Cited by: 15
Related to: 10
FWCI: 3.04
Citation percentile (by year/subfield): 82.14
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Sustainable Development Goal Good health and well-being
Open Access status: green