Atlastin-1, is a protein that in humans is encoded by the ATL1 gene.[1][2][3][4]

References

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  1. ^ Zhao X, Alvarado D, Rainier S, Lemons R, Hedera P, Weber CH, et al. (November 2001). "Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia". Nature Genetics. 29 (3): 326–31. doi:10.1038/ng758. PMID 11685207. S2CID 3154239.
  2. ^ Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J (October 1993). "Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q". Nature Genetics. 5 (2): 163–7. doi:10.1038/ng1093-163. PMID 8252041. S2CID 28541700.
  3. ^ Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, et al. (January 1995). "Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity". American Journal of Human Genetics. 56 (1): 183–7. PMC 1801298. PMID 7825576.
  4. ^ "Entrez Gene: SPG3A spastic paraplegia 3A (autosomal dominant)".
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Further reading

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