Acinar Dysplasia in a Full-Term Newborn with a NKX2.1 Variant
This study is the first to extend the phenotype of NKX2.1 pathogenic variant, to a fatal form of AcDys.PMID:38035569 | DOI:10.1159/000534076
Source: Neonatology - Category: Perinatology & Neonatology Authors: Yohan Soreze Nadia Nathan Julien Jegard Erik Hervieux Pauline Clermidi Chiara Sileo Camille Louvrier Marie Legendre Aurore Coulomb L'Hermin é Source Type: research
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