A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family
Titel:
A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family
Auteur:
Jelani, Musharraf Kang, Changsoo Mohamoud, Hussein Sheikh Ali Al-Rehaili, Rayan Almramhi, Mona Mohammad Serafi, Rehab Yang, Huanming Al-Aama, Jumana Yousuf Naeem, Muhammad Alkhiary, Yaser Mohammad