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MAST SYNDROME

Known as: SPASTIC PARAPLEGIA 21, AUTOSOMAL RECESSIVE, SPG21 
 
National Institutes of Health

Papers overview

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Review
2012
Review
2012
Hereditary spastic paraplegia (SPG) is a clinically and genetically heterogeneous group of neurodegenerative disorders that are… Expand
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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… Expand
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2010
2010
Mast syndrome (SPG21) is a childhood-onset, autosomal recessive, complicated form of hereditary spastic paraplegia (HSP… Expand
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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… Expand
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Highly Cited
2009
Highly Cited
2009
Normalization of mRNA levels using endogenous reference genes (ERGs) is critical for an accurate comparison of gene expression… Expand
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2009
2009
Mast syndrome (SPG21) is an autosomal-recessive complicated form of hereditary spastic paraplegia characterized by dementia, thin… Expand
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2007
2007
Hereditary spastic paraplegia (HSP) type 15 is an autosomal recessive (AR) form of complicated HSP mainly characterized by slowly… Expand
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2005
2005
The term hereditary spastic paraplegia (HSP) is used to describe a group of clinically and genetically heterogeneous disorders in… Expand
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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… Expand
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1967
1967
MANY aspects of the nosology of hereditary degenerative disorders of the nervous system remain obscure, and as yet no adequate… Expand
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