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SPG21 gene

Known as: MASPARDIN, MAST, SPG21 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (1)

Genes
MAST SYNDROMESPG7 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21
SPG21, also known as Mast Syndrome (MIM 248900), is an ultra-rare autosomal recessive complicated form of hereditary spastic… 
2016
2016
Supplementary Material for: Loss of Maspardin Attenuates the Growth and Maturation of Mouse Cortical Neurons
2015
2015
Novel compound heterozygous ALS2 mutations in two Chinese siblings with infantile ascending hereditary spastic paralysis
Mutations in ALS2 are responsible for three types of rare autosomal recessive disorders involving retrograde degeneration of… 
Highly Cited
2014
Highly Cited
2014
A Novel α/β-Hydrolase Gene IbMas Enhances Salt Tolerance in Transgenic Sweetpotato
Salt stress is one of the major environmental stresses in agriculture worldwide and affects crop productivity and quality. The… 
2014
2014
Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses
Hereditary spastic paraplegia (HSP) is one of the most genetically heterogeneous neurodegenerative disorders characterized by… 
2014
2014
SPG15: a cause of juvenile atypical levodopa responsive parkinsonism
Autosomal recessive hereditary spastic paraplegias with thin corpus callosum (AR HSP-TCC) are rare and complex neurodegenerative… 
2008
2008
Complicated autosomal recessive hereditary spastic paraplegia
Hereditary spastic paraplegia (HSP) has emerged as one of the most genetically heterogeneous neurodegenerative disorders. Almost… 
2007
2007
The role of hereditary spastic paraplegia related genes in multiple sclerosis
Multiple sclerosis (MS) is a common inflammatory disease of the central nervous system unsurpassed for its variability in disease… 
2005
2005
Complicated Hereditary Spastic Paraplegia with Thin Corpus Callosum (HSP‐TCC) and Childhood Onset
SPG21 
2001
2001
Cloning of ACP33 as a Novel Intracellular Ligand of CD4*
CD4 recruitment to T cell receptor (TCR)-peptide-major histocompatibility class II complexes is required for stabilization of low… 
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