Biallelic HMGXB4 loss-of-function variant causes intellectual disability, developmental delay, and dysmorphic features

Autor: Al Mutairi, Fuad a, b, ⁎, Joueidi, Faisal c, Alshalan, Maha a, Aloyouni, Essra b, Ballow, Mariam b, Aldrees, Mohammed b, Al Abdulrahman, Abdulkareem b, Al Tuwaijri, Abeer b, d, Abbas, Safdar e, Umair, Muhammad b, Alfadhel, Majid a, b
Zdroj: In Heliyon 15 August 2024 10(15)
Databáze: ScienceDirect