A Novel Homozygous HERC2 c.4660C>T (p. Arg1554Ter) Variant in an Infant with Severe Neurodevelopmental Disorder and Diffuse Osteopenia: A Case Report Manuscript Number2026/AJPR/165661 JournalAsian Journal of Pediatric Research AuthorsA. Moustapha, A. Laaraj, A. Radi, R. Abikassem Back to Journal