Correction: Nephrology 22, 261 (2021)
https://doi.org/10.1186/s12882-021-02466-z
Following publication of the original article [1], we found that there were misprint in the Fig. 2a. The correct Fig. 2 is given below:
Fig. 2.
Genetic analysis of the NPHP1 gene. a No exons from NPHP1 were amplified in this patient. b Multiplex ligation-dependent probe amplification analysis indicated complete deficiency of the NPHP1 gene
The original article has been corrected.
Reference
- 1.Akira M, et al. Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report. BMC Nephrol. 2021;22:261. doi: 10.1186/s12882-021-02466-z. [DOI] [PMC free article] [PubMed] [Google Scholar]