SPG21 gene

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

Topic mentions per year

Topic mentions per year

2003-2016
012320032016

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
BACKGROUND Mast syndrome, an autosomal recessive, progressive form of hereditary spastic paraplegia, is associated with mutations… (More)
Is this relevant?
2014
2014
Hereditary spastic paraplegia (HSP) is one of the most genetically heterogeneous neurodegenerative disorders characterized by… (More)
  • table 2
Is this relevant?
2011
2011
Mutations in the SPG3A gene cause the most frequent autosomal dominant (AD) type of pure hereditary spastic paraplegia (HSP) with… (More)
  • figure 1
  • table 1
Is this relevant?
2010
2010
Mast syndrome (SPG21) is a childhood-onset, autosomal recessive, complicated form of hereditary spastic paraplegia (HSP… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2009
2009
Normalization of mRNA levels using endogenous reference genes (ERGs) is critical for an accurate comparison of gene expression… (More)
  • figure 1
  • table 1
  • table 1
  • figure 2
  • table 2
Is this relevant?
2009
2009
Mast syndrome (SPG21) is an autosomal-recessive complicated form of hereditary spastic paraplegia characterized by dementia, thin… (More)
  • figure 1
  • figure 2
  • figure 4
  • figure 5
  • figure 6
Is this relevant?
2006
2006
Multiple sclerosis (MS) is a common inflammatory disease of the central nervous system unsurpassed for its variability in disease… (More)
  • table 1
  • table 2
  • table 2
  • table 3
  • table 3
Is this relevant?
2005
2005
T he term hereditary spastic paraplegia (HSP) is used to describe a group of clinically and genetically heterogeneous disorders… (More)
  • table 1
  • figure 1
  • figure 2
Is this relevant?
2005
2005
The hereditary spastic paraplegias (HSPs) are a group of rare disorders with the predominant clinical feature of progressive… (More)
Is this relevant?
Highly Cited
2003
Highly Cited
2003
Mast syndrome is an autosomal recessive, complicated form of hereditary spastic paraplegia with dementia that is present at high… (More)
Is this relevant?