Table 1.

Mutation screening results.

Causative gene	N	%
NPHS2	156	41.8
WT1	59	15.8
NPHS1	47	12.6
SMARCAL1	20	5.4
PLCE1	14	3.8
ADCK4	13	3.5
COL4A5	11	1.3
LMX1B	10	2.7
INF2	8	2.1
LAMB2	8	2.1
COQ6	6	1.6
MYO1E	6	1.6
PTPRO	5	1.3
TRPC6	3	0.8
CLCN5	2	0.5
COQ2	2	0.5
PAX2	2	0.5
ACTN4	1	0.3
COL4A3	1	0.3
Others	4	1.1
All	373	100

Genetic diagnoses in 373 of 1,554 genetically screened children with hereditary SRNS (24%).