Table 1.

Summary of lines.

iPSC line names	Abbreviation in figures	Gender	Age	Ethnicity	Genotype of locus	Disease
NIAi001-A	I2020T PL2F4	Female	Neonate	Unknown	I2020T homozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-B	I2020T PL2D7	Female	Neonate	Unknown	I2020T heterozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-C	G2019S PL2A9	Female	Neonate	Unknown	G2019S homozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-D	G2019S PL2H7	Female	Neonate	Unknown	G2019S heterozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-E	Y1699C PL3H2	Female	Neonate	Unknown	Y1699C homozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-F	Y1699C PL2H7	Female	Neonate	Unknown	Y1699C heterozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-G	R1441C PL2F5	Female	Neonate	Unknown	R1441C homozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-H	R1441C PL3C2	Female	Neonate	Unknown	R1441C heterozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-I	N1437H PL3D7	Female	Neonate	Unknown	N1437H homozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-J	N1437H PL3F5	Female	Neonate	Unknown	N1437H heterozygous mutation in LRRK2 gene	Parkinson disease
NIAi001-K	K1906M PL2H7	Female	Neonate	Unknown	K1906M homozygous mutation in LRRK2 gene	NIAi001-K
NIAi001-L	T1348N PL1B6	Female	Neonate	Unknown	T1348N homozygous mutation in LRRK2 gene	NIAi001-L
NIAi001-M	LRRK2 KO PL1C4	Female	Neonate	Unknown	c.5694_5697delTGAA (p.Tyr1898Ter) and c.4016_4985del (p.Ile1339LysfsX12)	NIAi001-M
NIAi001-N	LRRK2 KO PL1C6	Female	Neonate	Unknown	c.4015_4018delATTG (p.Ile1339TrpfsX15) and c.4016_4985del (p.Ile1339LysfsX12) mutations in LRRK2 gene