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Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes

Crossref DOI link: https://doi.org/10.1007/s10157-021-02135-3

Published Online: 2021-09-18

Published Print: 2022-02

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Ishiko, Shinya

Morisada, Naoya https://orcid.org/0000-0002-9676-865X
Kondo, Atsushi

Nagai, Sadayuki

Aoto, Yuya

Okada, Eri

Rossanti, Rini

Sakakibara, Nana

Nagano, China

Horinouchi, Tomoko

Yamamura, Tomohiko

Ninchoji, Takeshi

Kaito, Hiroshi

Hamada, Riku

Shima, Yuko

Nakanishi, Koichi

Matsuo, Masafumi

Iijima, Kazumoto

Nozu, Kandai
Funding

Funding for this research was provided by:

health labor sciences research grant (H24-nanchi-ippan-041, H29-nanchi-ippan-039)

japan society for the promotion of science (JP15K09261, 18K08243)
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Text and Data Mining valid from 2021-09-18

Version of Record valid from 2021-09-18
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Article History

Received: 18 June 2021

Accepted: 7 September 2021

First Online: 18 September 2021

Declarations

:

: K.I. has received grant support from Daiichi Sankyo Co., Ltd. and Zenyaku Kogyo Co., Ltd. M. M discloses being employed by Kobe Gakuin University, which received funding from KNC Laboratories Inc. (Kobe, Japan). The author further discloses being a scientific adviser for Daiichi-Sankyo Co. (Tokyo, Japan) and JCR Pharma Co. (Ashiya, Japan).

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