Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health
Reference15 articles.
1. Classification of the hereditary ataxias and paraplegias;Harding;Lancet,1983
2. A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum;Blumkin;J Neurol Sci,2011
3. Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study;Erichsen;Brain,2009
4. Hereditary spastic paraplegia: from genes, cells and networks to novel pathways for drug discovery;Mackay-Sim;Brain Sci,2021
5. Gamma-synergin: an EH domain-containing protein that interacts with gamma-adaptin;Page;J Cell Biol,1999
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