Characterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia (vol 16, pg 97, 2015)
Por:
Lopez, E, Casasnovas, C, Gimenez, J, Matilla-Duenas, A, Sanchez, I and Volpini, V
Publicada:
1 ene 2022
Ahead of Print:
1 nov 2021
Resumen:
Filiaciones:
Lopez, E:
Inst Recerca Biomed Bellvitge IDIBELL, Ctr Diagnost Genet Mol CDGM, Gran Via 199, Barcelona 08907, Spain
Casasnovas, C:
Inst Recerca Biomed Bellvitge IDIBELL, Ctr Diagnost Genet Mol CDGM, Gran Via 199, Barcelona 08907, Spain
Hosp Univ Bellvitge, IDIBELL, Neurol Dept, Neuromuscular Unit, C Feixa Llarga S-N, Barcelona 08907, Spain
Gimenez, J:
Inst Recerca Biomed Bellvitge IDIBELL, Ctr Diagnost Genet Mol CDGM, Gran Via 199, Barcelona 08907, Spain
:
Germans Trias & Pujol IGTP, Hlth Sci Res Inst, Bas Translat & Mol Neurogenet Res Unit Neurosci, Barcelona, Spain
Univ Autonoma Barcelona, Neurosci Dept, Barcelona, Spain
:
Germans Trias & Pujol IGTP, Hlth Sci Res Inst, Bas Translat & Mol Neurogenet Res Unit Neurosci, Barcelona, Spain
Univ Autonoma Barcelona, Neurosci Dept, Barcelona, Spain
Boston Univ, Sch Med BUMC, Dept Anat & Neurobiol, Lab Syst Mol Signalling & Chem Biol, Boston, MA 02215 USA
Volpini, V:
Inst Recerca Biomed Bellvitge IDIBELL, Ctr Diagnost Genet Mol CDGM, Gran Via 199, Barcelona 08907, Spain
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