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SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE

Known as: SPG55 
National Institutes of Health

Related topics

Related topics

7 relations
Autosomal recessive inheritanceAxonal neuropathyClonusCongenital clubfoot

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Clinical utility gene card for: inherited optic neuropathies including next-generation sequencing-based approaches
: 
Highly Cited
2012
Highly Cited
2012
A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)
Background Autosomal recessive hereditary spastic paraplegias (AR-HSP) constitute a heterogeneous group of neurodegenerative… 
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