TY  - GEN
AU  - Mademan,Inès
AU  - Deconinck,Tine
AU  - Dinopoulos,Argirios
AU  - Voit,Thomas
AU  - Schara,Ulrike
AU  - Devriendt,Koenraad
AU  - Meijers,Björn
AU  - Lerut,Evelyne
AU  - De Jonghe,Peter
AU  - Baets,Jonathan
TI  - De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy
SN  - 1526-632X
PY  - 2014///0121
KW  - Adolescent
KW  - Adult
KW  - Charcot-Marie-Tooth Disease
KW  - complications
KW  - DNA Mutational Analysis
KW  - Family Health
KW  - Female
KW  - Formins
KW  - Glomerulosclerosis, Focal Segmental
KW  - Humans
KW  - Male
KW  - Microfilament Proteins
KW  - genetics
KW  - Models, Molecular
KW  - Mutation
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/01.wnl.0000436615.58705.c9
ER  -