Correction to: Characterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia.

Neurogenetics

Centre de Diagnòstic Genètic i Molecular (CDGM)-Institut de Recerca Biomèdica de Bellvitge (IDIBELL), Gran Via 199, 08907, L'Hospitalet de Llobregat, Barcelona, Spain.

Published: January 2022

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http://dx.doi.org/10.1007/s10048-021-00654-5DOI Listing

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