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SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE

Known as: SPG48 
National Institutes of Health

Related topics

Related topics

3 relations
Autosomal recessive inheritanceLower limb muscle weaknessUrinary Incontinence

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Faculty Opinions recommendation of Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48).
  • S. Tisch
  • Faculty Opinions – Post-Publication Peer Review…
  • 2018
  • Corpus ID: 81522547
2016
2016
Erratum: Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48).
  • Neurology: Genetics
  • 2016
  • Corpus ID: 261715808
[This corrects the article on p. e98 in vol. 2, PMID: 27606357.]. 
2011
2011
And Now There Are Five: A New Player in Intracellular Trafficking Pathways
​PeeringPeering at a cell through a microscope reveals a hotbed of seemingly random activity, as proteins zip here and there. But… 
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