MAST SYNDROME

Known as: SPG21, Spastic Paraplegia 21, Autosomal Recessive 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2005-2017
012320052017

Papers overview

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2014
2014
Mutations in ALS2 are responsible for three types of rare autosomal recessive disorders involving retrograde degeneration of… (More)
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Review
2012
Review
2012
Hereditary spastic paraplegia (SPG) is a clinically and genetically heterogeneous group of neurodegenerative disorders that are… (More)
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2011
2011
Mutations in the SPG3A gene cause the most frequent autosomal dominant (AD) type of pure hereditary spastic paraplegia (HSP) with… (More)
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2010
2010
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) maps to the SPG11 locus in the majority of… (More)
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2010
2010
Mast syndrome (SPG21) is a childhood-onset, autosomal recessive, complicated form of hereditary spastic paraplegia (HSP… (More)
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2010
2010
OBJECTIVE To investigate the effect of hepatitis B virus(HBV) X gene on the expression of SPG21. METHODS The expressions of… (More)
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2009
2009
Normalization of mRNA levels using endogenous reference genes (ERGs) is critical for an accurate comparison of gene expression… (More)
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2009
2009
Mast syndrome (SPG21) is an autosomal-recessive complicated form of hereditary spastic paraplegia characterized by dementia, thin… (More)
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2009
2009
SPG4-related hereditary spastic paraplegia is associated with posterior fossa abnormalities that are part of the Dandy–Walker… (More)
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2005
2005
T he term hereditary spastic paraplegia (HSP) is used to describe a group of clinically and genetically heterogeneous disorders… (More)
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