# Correction: Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other origins

**Authors:** Agata Zygmunt-Górska, Małgorzata Wójcik, Aleksandra Gilis-Januszewska, Anna Starmach, Mirosław Bik-Multanowski, Jerzy B. Starzyk

PMC · DOI: 10.1007/s42000-024-00543-0 · 2024-03-18

## Full-text entities

- **Genes:** PROP1 (PROP paired-like homeobox 1) [NCBI Gene 5626] {aka CPHD2, PROP-1}
- **Diseases:** pituitary hormone deficiency (MESH:C580003)

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Source: https://tomesphere.com/paper/PMC11219399