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SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE
Known as:
SPG72
National Institutes of Health
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Related topics
Related topics
4 relations
Autosomal dominant inheritance
Autosomal recessive inheritance
Muscular stiffness
REEP2 gene
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2017
2017
De novo REEP2 missense mutation in pure hereditary spastic paraplegia
R. Roda
,
A. Schindler
,
C. Blackstone
Annals of Clinical and Translational Neurology
2017
Corpus ID: 28272222
Alterations in proteins that regulate endoplasmic reticulum morphology are common causes of hereditary spastic paraplegia (SPG1…
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