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

López, Eva; Casasnovas, Carlos; Giménez, Javier; Matilla-Dueñas, Antoni; Sánchez, Ivelisse; Volpini, Víctor

López, Eva; Casasnovas, Carlos; Giménez, Javier; Matilla-Dueñas, Antoni; Sánchez, Ivelisse; Volpini, Víctor.

Affiliation

López E; Centre de Diagnòstic Genètic i Molecular (CDGM)-Institut de Recerca Biomèdica de Bellvitge (IDIBELL), Gran Via 199, 08907, L'Hospitalet de Llobregat, Barcelona, Spain. eltoledano@gmail.com.
Casasnovas C; Centre de Diagnòstic Genètic i Molecular (CDGM)-Institut de Recerca Biomèdica de Bellvitge (IDIBELL), Gran Via 199, 08907, L'Hospitalet de Llobregat, Barcelona, Spain.
Giménez J; Neuromuscular Unit, Neurology Department, Hospital Universitari de Bellvitge, IDIBELL, C/Feixa Llarga s/n., 08907, L'Hospitalet de Llobregat, Barcelona, Spain.
Matilla-Dueñas A; Centre de Diagnòstic Genètic i Molecular (CDGM)-Institut de Recerca Biomèdica de Bellvitge (IDIBELL), Gran Via 199, 08907, L'Hospitalet de Llobregat, Barcelona, Spain.
Sánchez I; Basic, Translational and Molecular Neurogenetics Research Unit in Neurosciences, Health Sciences Research Institute, Germans Trias y Pujol (IGTP), Badalona, Barcelona, Spain.
Volpini V; Neuroscience Department, Universitat Autònoma de Barcelona, Barcelona, Spain.

Neurogenetics ; 23(1): 79, 2022 Jan.

Article in En | MEDLINE | ID: mdl-34755250

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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Neurogenetics Journal subject: GENETICA / NEUROLOGIA Year: 2022 Type: Article Affiliation country: Spain

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