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Updated: Dec 12, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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LEOPARD Syndrome with PTPN11 Gene Mutation in Three Family Members Presenting with Different Phenotypes

Nuha Alfurayh1, Fahad Alsaif1, Nouf Alballa1

  • 1Department of Dermatology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Journal of Pediatric Genetics
|August 9, 2020
PubMed

Keywords:
LEOPARD syndromePTPN11multiple lentigines

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