Table 2 Summary of changes

From: Author Correction: Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations

Corrections

Original

Corrected

Affected parts of the original Letter

cED4 haplotype

H49

B2k

Table 1, Supplementary Tables 1, 3, 4 and 5, Fig. 3 and Extended Data Fig. 3a, 5a and 7b

hED4 haplotype

B2k

H49

hED6 haplotype

V3

H1g

Donor mtDNA haplotype for NT-ES5

D1a

D4a

Nucleotide at mt11253 for H6a haplotype of carrier 1

T

C

Supplementary Table 1

Nucleotide at mt11812 for T2b haplotype in carrier 3

A

G

Nucleotide at mt3107 for U5a haplotype in 33 SNPs-2 (32 SNPs)

A

Deleted

Distance between T2 and T2b in carrier 3

22

21

Table 1, Supplementary Table 1 and Extended Data Fig. 3a

Distance between U5a and H1g in 33 SNPs-2 (32 SNPs)

33

32

B2k haplotype at position mt11177

T

‘Summary’ tab in Supplementary Table 5

Typographic errors in assignment of egg donor IDs

hED7

hED10

Supplementary Tables 1, 3, 4 and 5

hED10

hED7

hED6

hED9

hED9

hED6

hED8

hED11

hED11

hED5

hED5

hED8

SNP differences in D-loop region between H49 and B2k

14

5

Table 1 and Supplementary Table 1

SNP differences in coding region between D4a and A2g

18

19