A novel mutation in the TM6 domain of GABBR2 leads to a Rett-like phenotype
Journal article published in 2018 by
M. L. Vuillaume,
M. Jeanne,
L. Xue,
S. Blesson,
A. S. Denommé Pichon 
,
S. Alirol,
C. Brulard,
E. Colin,
B. Isidor,
B. Gilbert Dussardier,
S. Odent,
P. Parent,
A. Donnart,
R. Redon,
S. Bézieau
and other authors.
,
S. Alirol,
C. Brulard,
E. Colin,
B. Isidor,
B. Gilbert Dussardier,
S. Odent,
P. Parent,
A. Donnart,
R. Redon,
S. Bézieau
and other authors.
