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Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection

Crossref DOI link: https://doi.org/10.1007/s10072-023-06960-0

Published Online: 2023-07-15

Published Print: 2023-12

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

Authors

Tehrani Fateh, Sahand https://orcid.org/0009-0002-8903-2713
Bagheri, Saman https://orcid.org/0000-0003-0093-6995
Sadeghi, Hossein https://orcid.org/0000-0001-9599-6151
Salehpour, Shadab https://orcid.org/0000-0002-0277-809X
Fazeli Bavandpour, Fatemehsadat

Sadeghi, Behnia

Jamshidi, Sanaz

Tonekaboni, Seyed Hassan https://orcid.org/0000-0003-0853-8465
Mirfakhraie, Reza https://orcid.org/0000-0003-1709-8975
Miryounesi, Mohammad https://orcid.org/0000-0003-4705-3794
Ghasemi, Mohammad-Reza https://orcid.org/0000-0002-3183-5495
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Text and Data Mining valid from 2023-07-15

Version of Record valid from 2023-07-15
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Article History

Received: 29 June 2023

Accepted: 10 July 2023

First Online: 15 July 2023

Declarations

:

: This study was approved by the Research Ethics Committee of the Faculty of Medicine, Shahid Beheshti University of Medical Sciences, and was conducted in accordance with the tenets of the Declaration of Helsinki. Informed consent was obtained from parents.

: All the contributing authors agreed for the publication in this journal.

: The authors declare no competing interests.

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