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SPG9 gene

Known as: SPG9, spastic paraplegia 9 (autosomal dominant) 
 
National Institutes of Health

Papers overview

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2020
2020
The ALDH18A1 gene, encoding delta-1-pyrroline-5-carboxylate synthase (P5CS), is responsible for an autosomal recessive disease… Expand
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2019
2019
Abstract In 2015–2016, we and others reported ALDH18A1 mutations causing dominant (SPG9A) or recessive (SPG9B) spastic paraplegia… Expand
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2018
2018
Hereditary spastic paraplegias (HSPs) are characterized by various inherited disorders in which weakness and spasticity of the… Expand
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2018
2018
Hereditary spastic paraplegia (HSP) is one of the most genetically heterogeneous neurological disorders. HSP is classified as… Expand
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2008
2008
BACKGROUND AND PURPOSE The hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders… Expand
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2008
2008
BACKGROUND Hereditary spastic paraplegia (HSP) is a group of inherited neurodegenerative disorders with the shared… Expand
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2004
2004
The hereditary spastic paraplegias (HSPs) are a group of clinically and genetically heterogeneous disorders characterized by… Expand
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2003
2003
We have recently mapped a new rare form of spastic paraplegia complicated by bilateral cataracts, gastroesophageal reflux with… Expand
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2001
2001
Editor—Recently, Reid et al 1 reported reduction of the chromosome 12q locus for autosomal dominant hereditary spastic paraplegia… Expand
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2000
2000
Hereditary spastic paraplegia (HSP) is a genetically heterogeneous disorder characterised by progressive spasticity of the lower… Expand
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