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Spastic Paraplegia 33, Autosomal Dominant

Known as: SPG33 
National Institutes of Health

Related topics

Related topics

5 relations
Autosomal dominant inheritanceCongenital clubfootLower limb muscle weaknessZFYVE27 gene

Broader (1)

Spastic Paraplegia, Hereditary

Papers overview

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2008
2008
Refinement of the SPG9 locus on chromosome 10q23.3‐24.2 and exclusion of candidate genes
Background and purpose:  The hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders… 
2008
2008
Novel mutation in the SPAST gene in a patient with spastic paraparesis
gene,is the most common cause ofdominantly inherited HSP,repre-senting approximately 40% offamilial,and 5–10% of sporadiccases [3… 
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