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SPG21 gene

Known as: MASPARDIN, MAST, SPG21 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (1)

Genes
MAST SYNDROMESPG7 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21
SPG21, also known as Mast Syndrome (MIM 248900), is an ultra-rare autosomal recessive complicated form of hereditary spastic… 
2016
2016
Supplementary Material for: Loss of Maspardin Attenuates the Growth and Maturation of Mouse Cortical Neurons
2016
2016
P33 of Helicoverpa armigera single nucleocapsid nucleopolyhedrovirus is a functional homolog of AcP33
2012
2012
Characterization of maspardin, responsible for human Mast syndrome, in an insect species and analysis of its evolution in metazoans
Mast syndrome is a complicated form of human hereditary spastic paraplegias, caused by a mutation in the gene acid cluster… 
Review
2010
Review
2010
Studies on hereditary spastic paraplegia proteins
The hereditary spastic paraplegias (HSPs) are a clinically and genetically diverse group of inherited neurological disorders that… 
2008
2008
Complicated autosomal recessive hereditary spastic paraplegia
Hereditary spastic paraplegia (HSP) has emerged as one of the most genetically heterogeneous neurodegenerative disorders. Almost… 
2008
2008
Zellspezifische Expression von Maspardin in murinem und humanen postmortalen Rückenmark – Bedeutung für die hereditäre spastische Spinalparalyse 21
2005
2005
Complicated Hereditary Spastic Paraplegia with Thin Corpus Callosum (HSP‐TCC) and Childhood Onset
SPG21 
2003
2003
Maspardin is mutated in Mast syndrome, a form of hereditary spastic paraplegia associated with dementia.
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