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For: Ma N, Li ZW, Liu JJ, Liu XG, Zhou X, Wang BW, Li YL, Zhang TC, Xie P. RAF1 mutation expands the cardiac phenotypic spectrum of Noonan syndrome: A case report. World J Cardiol 2025; 17(6): 106525 [PMID: 40575432 DOI: 10.4330/wjc.v17.i6.106525]
URL: https://www.wjgnet.com/1949-8462/full/v17/i6/106525.htm
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Sanae Kheir, Jihane Ahmidi, Mariam Tajir, Maria Rkain, Abdeladim Babakhouya. Noonan Syndrome Type 5 Diagnosed by Next-Generation Sequencing: A Report of a Rare Pediatric Case. Cureus 2026;  doi: 10.7759/cureus.115089
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