Correction: Deleterious Rare Variants Reveal Risk for Loss of GABA_A Receptor Function in Patients with Genetic Epilepsy and in the General Population

In Table 2, three variants corresponding to the GABRP gene were incorrectly described. The R200H variant should be R200H/C, the S293P variant should be R293C, and the R389N variant should be D389N. Please see the corrected Table 2 here.

Table 2. Unique GABR variants from GECs reported in the 237 ion channel genes project¹.

¹GECs = genetic epilepsy cases [20]. *GABR variants characterized in this study.

GABR gene	Variant	Occurrence of variants among GECs
GABRA1	T20I*	1
GABRA4	H372P*	1
GABRA5	W280R*	3
GABRA5	P453L*	1
GABRB2	R293W*	1
GABRG3	A303T*	1
GABRA4	A19T*	1
GABRA5	V204I*	1
GABRA5	S402A*	1
GABRA6	Q237R*	1
GABRB1	H421Q*	1
GABRB2	R354C*	2
GABRG1	S16R*	1
GABRG1	S414N*	1
GABRE	R472H	1
GABRE	S484L	1
GABRP	R200H/C	2
GABRP	S292P	1
GABRP	R293C	1
GABRP	D389N	1
GABRR2	R287H	1
GABRR2	V294I	2
GABRE	R452G	1
GABRP	V349A	5