FBXO22 Deficiency Defines a Pleiotropic Syndrome of Growth Restriction and Multi-System Anomalies Associated with a Unique Epigenetic Signature
Navin B. Ramakrishna,Yoshikazu Johmura,Nur Ain Ali, Umar B Mohamad Sahari,Malak Alghamdi,Peter Bauer,Suliman Khan,Natalia Ordonez,Mariana Ferreira,Jorge Pinto Basto,Fowzan S Alkuraya, Eissa Ali Faqeih, Mari Mori,Naif AM Almontashiri,Aisha Al Shamsi, Gehad ElGhazali, Hala Abu Subieh,Mode Al Ojaimi,Ayman W. El-Hattab, Said Ahmed Said Al-Kindi,Nadia Alhashmi, Fahad Alhabshan, Abdulaziz Al Saman, Hala Tfayli, Mariam Arabi, Simone Khalifeh,Alan Taylor,Majid Alfadhel,Ruchi Jain, Shruti Sinha,Shruti Shenbagam,Revathy Ramachandran, Umut Altunoglu,Anju Jacob,Nandu Thalange, Jay W Shin,Almundher Al-Maawali, Azza Al-Shidhani,Amna Al-Futaisi,Fatma Rabea, Ikram Chekroun, Mohamed Al Marri,Tomohiko Ohta,Makoto Nakanishi,Alawi Alsheikh-Ali,Fahad R Ali, Aida M Bertoli-Avella,Bruno Reversade,Ahmad N Abou Tayoun crossref（2024）
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