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. 2023 Nov 7;24:327. doi: 10.1186/s12882-023-03352-6

Correction: Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report

Maiko Akira 1, Hitoshi Suzuki 1,, Arisa Ikeda 1, Masako Iwasaki 1, Daisuke Honda 1, Hisatsugu Takahara 1, Hisaki Rinno 1, Shigeki Tomita 2, Yusuke Suzuki 3
PMCID: PMC10630989  PMID: 37936088

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.

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]

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