Novel insight into the phenotype of microcephaly 19 in the patient with missense COPB2 mutation

Autor: Shiri, Amirmasoud, Jafari Khamirani, Hossein, Kamal, Neda, manoochehri, Jamal, Dianatpour, Mehdi, Tabei, Seyed Mohammad Bagher, Dastgheib, Seyed Alireza
Zdroj: In European Journal of Medical Genetics October 2023 66(10)
Databáze: ScienceDirect