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SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE

Known as: SPG78 
National Institutes of Health

Related topics

Related topics

13 relations
ATP13A2, GLN122TERAbnormal pyramidal signsAggressive behaviorAtaxia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Loss-of-function mutations in the ATP 13 A 2 / PARK 9 gene cause complicated hereditary spastic paraplegia ( SPG 78 )
PARK9 gene cause complicated hereditary spastic paraplegia (SPG78) Alejandro Estrada-Cuzcano, Shaun Martin, Teodora Chamova… 
2017
2017
Novel form of complicated hereditary spastic paraplegia (SPG78), due to mutations in the ATP13A2/PARK9 gene
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