Title: De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy
Authors: Mademan, Inès ×
Deconinck, Tine
Dinopoulos, Argirios
Voit, Thomas
Schara, Ulrike
Devriendt, Koenraad
Meijers, Björn
Lerut, Evelyne
De Jonghe, Peter
Baets, Jonathan #
Issue Date: Nov-2013
Publisher: Advanstar Communications
Series Title: Neurology vol:81 issue:22 pages:1953-8
Abstract: Identification of mutations in the inverted formin-2 (INF2) gene in patients with Charcot-Marie-Tooth (CMT) disease combined with focal segmental glomerulosclerosis (FSGS) in order to expand the genetic and phenotypic spectrum.
ISSN: 0028-3878
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Department of Human Genetics - miscellaneous
× corresponding author
# (joint) last author

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