A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family

por Ahmad, Safeer, Ali, Muhammad Zeeshan, Abbasi, Sumra Wajid, Abbas, Safdar, Ahmed, Iftikhar, Abbas, Shakil, Nawaz, Shoaib, Ziab, Mubarak, Ahmed, Ikhlak, Fakhro, Khalid A., Khan, Muzammil Ahmad, Akil, Ammira Al-Shabeeb
Publicado 2023