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Genotype-phenotype study and expansion of ARL6IP1-related complicated hereditary spastic paraplegia. Clinical genetics Cao, Y., Manning, M., Pope, K., He, W., Vetrini, F., Siskind, C., Rosenfeld, J. A., Yang, Y., Xiao, R. 2020
View details for DOI 10.1111/cge.13870
View details for PubMedID 33188530