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ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2023

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

Sahand Tehrani Fateh et al.PubMed ↗Publisher ↗

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3 papers cite it

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2025
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Full record →Abstract, authors, funding and every citing paper · PMID 37452996