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. 2019 Jul 10;19:156. doi: 10.1186/s12883-019-1390-7

Table 2.

CLCN2 mutations of the reported patients with CLCN2-related leukoencephalopathy

Case Exon DNA Protein Genotype
1 1 c.61dup p.Leu21ProfsTer27 Homozygous
2 c.1412G > A p.Arg471His Homozygous
3 p.Glu475LysfsTer79 Homozygous
4 p.Leu435ArgfsTer7 Compound heterozygous
5 16 c.1769A > C p.His590Pro Homozygous
6 c.1113delinsACTGCTCAT p.Ser375CysfsX6 Homozygous
7 c.1507G > A p.Gly503Arg Homozygous
8 15 c.709G > A p.Trp570X Homozygous
9 15 c.1709G > A p.Trp570X Homozygous
10 4 c.430_435del p.Leu144_Ile145del Homozygous
11 11; 2 to part of 6 c.1143delT; c.64–1107_639del p.Gly382AlafsX34; p.Met22LeufsX5 Heterozygous; heterozygous
12 14 c.1499C > T p.Ala500Val Homozygous
13 8 c.828dupG p.Arg277AlafsX23 Homozygous
14 20 c.2257C > T p.Arg753Ter Homozygous

1. Hoshi et al. [2018]

2–4. Zeydan et al. [2017]

5. Giorgio et al. [2017]

6. Hanagasi et al. [2015]

7. Di Bella et al. [2014]

8–13. Depienne et al. [2013]

14. The case of our study