摘要：Correction to:
Scientific Reports
https://doi.org/10.1038/s41598-021-81015-y, published online 11 February 2021
The original version of this Article contained errors.
In Table 1, the value given for the Status of Family no. #9 was incorrect.
“Dead (2 y 10 m)”
now reads:
“Dead (2 y 9 m)”
In Figure 2, panel G, pro-band I, the square indicating father (3) was incorrectly given as a circle. In addition, the circle indicating mother (4) was omitted. In pro-band IIII, the description under the triangle was incorrectly included.
In panel I, pro-band II, the square indicating male (1) was incorrectly given as a circle.
In panel L, pro-band I, the square indicating the father (1) was incorrectly shown as being a carrier of the pathological variant.
The original Figure
2 and accompanying legend appears below.
Figure 2
Family tree of 13 probands. One family had X chromosome-linked gene mutation; the other 12 families had autosomal recessive gene mutations. In our cohort, there was no consanguineous couple.
Fam family,
CM cardiomyopathy,
LIMD lethal infantile mitochondrial disease,
NLIMD non-lethal infantile mitochondrial disease,
LS Leigh syndrome,
HD hepatic disease,
MTDPS mitochondrial DNA depletion syndrome,
WT wild type,
m month,
d day,
y year.
The original Article has been corrected.
