A Compound Heterozygous Cathepsin C Mutations Causing Phenotypical Papillion Lafevre/Haim‐Munk Syndrome: A Case Report and Review of WES Findings

Fuente: Wiley Open Access

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Bibliographic Details
Main Authors:	Motaz Assas, Abdullah Hazzazi, Abdullah Alutaibi, Ameerah Aladwani, Arwa U. Alsaggaf, Bashayer Alshawi, Hassan Abed
Format:	Artículo Open Access
Published:	Wiley 2026
Subjects:	Special Care in Dentistry
Online Access:	Acceder al recurso
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