Published in Nat Genet on November 01, 1999
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Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domain. Proc Natl Acad Sci U S A (2011) 1.18
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein. Neurogenetics (2006) 1.15
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34. Am J Hum Genet (2000) 1.14
A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42). Am J Hum Genet (2008) 1.09
Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology. Hum Genet (2015) 1.09
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Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia. Clin Genet (2011) 0.95
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Identification of the Drosophila melanogaster homolog of the human spastin gene. Dev Genes Evol (2003) 0.91
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The role of ZFYVE27/protrudin in hereditary spastic paraplegia. Am J Hum Genet (2008) 0.91
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Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy. Am J Hum Genet (2016) 0.83
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