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1 research outputs found
EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss
Author
A Behlouli
A Imtiaz
+39 more
A Veske
AM Heer de
AU Rehman
C Petit
Christine Petit
Crystel Bonnet
CT Bladwin
CZ Seco
DN Furness
F Ammar-Khodja
F Denoyelle
Fatima Ammar-Khodja
FJ Castillo del
Gaelle M. Lefèvre
Hassina Ibrahim
HF Horn
HS Scott
I Ebermann
Jean-Pierre Hardelin
K Frei
M Bitner-Glindzicz
M Huang
M Schwander
Malika Dahmani
MH Chaleshtori
N Charizopoulou
N Grillet
N Offenhäuser
NE Morton
RWJ Collin
S Abe
S Delmaghani
S Delmaghani
T Walsh
U Manor
V Zampini
VB Piatto
Y Li
Zahia Mallek
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
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