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 |
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Zdroj: | In European Journal of Medical Genetics October 2023 66(10) |
Databáze: | ScienceDirect |
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