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Updated: Jun 2, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
06:41

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

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[Sotos syndrome: a novel nonsense mutation in NSD1 gene, presenting with neonatal cutis laxa]

E Cortès-Saladelafont1, K Arias-Sáez, D Esteban-Oliva

  • 1Servicio de Pediatría, Hospital Universitario Germans Trias i Pujol, Badalona, España.

Anales De Pediatria (Barcelona, Spain : 2003)
|April 13, 2011
PubMed

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