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SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE
Known as:
SPG61
National Institutes of Health
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Related topics
Related topics
3 relations
ARL6IP1 gene
Autosomal recessive inheritance
Muscle Spasticity
Papers overview
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2019
2019
A new case of infantile‐onset hereditary spastic paraplegia with complicated phenotype (SPG61) in a consanguineous Russian family
A. Chukhrova
,
I. A. Akimova
,
O. Shchagina
,
V. A. Kadnikova
,
O. Ryzhkova
,
A. Polyakov
European Journal of Neurology
2019
Corpus ID: 111390171
SPG61 (OMIM: 615685) is an extremely rare form of complicated hereditary spastic paraplegia [1,2]. To date, only one family with…
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2016
2016
ER-shaping proteins are required for ER and mitochondrial network organization in motor neurons.
P. C. Fowler
,
N. C. O'sullivan
Human Molecular Genetics
2016
Corpus ID: 37961608
Hereditary spastic paraplegias (HSPs) are a group of neurodegenerative disorders characterized by degeneration of the longest…
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