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SPG21 gene
Known as:
MASPARDIN
, MAST
, SPG21
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National Institutes of Health
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Related topics
Related topics
3 relations
Broader (1)
Genes
MAST SYNDROME
SPG7 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Supplementary Material for: Loss of Maspardin Attenuates the Growth and Maturation of Mouse Cortical Neurons
A. Davenport
,
A. Bivona
,
W. Latson
,
L. Lemanski
,
V. Cheriyath
2016
Corpus ID: 185656615
2012
2012
Characterization of maspardin, responsible for human Mast syndrome, in an insect species and analysis of its evolution in metazoans
T. Chertemps
,
N. Montagné
,
F. Bozzolan
,
Annick Maria
,
Nicolas Durand
,
M. Maïbèche-Coisné
Die Naturwissenschaften
2012
Corpus ID: 253640524
Mast syndrome is a complicated form of human hereditary spastic paraplegias, caused by a mutation in the gene acid cluster…
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Review
2010
Review
2010
Studies on hereditary spastic paraplegia proteins
C. Soderblom
2010
Corpus ID: 13710011
The hereditary spastic paraplegias (HSPs) are a clinically and genetically diverse group of inherited neurological disorders that…
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2008
2008
Zellspezifische Expression von Maspardin in murinem und humanen postmortalen Rückenmark – Bedeutung für die hereditäre spastische Spinalparalyse 21
J. S. Tjan
,
J. Zschüntzsch
,
P. Dibaj
,
S. Petri
,
F. Kirchhoff
,
C. Neusch
2008
Corpus ID: 71371224
2003
2003
Maspardin is mutated in Mast syndrome, a form of hereditary spastic paraplegia associated with dementia.
M. Simpson
,
C. Proukakis
,
H. Cross
,
M. Patton
,
A. Crosby
2003
Corpus ID: 74158510