Skip to Main Content

Paper Details

A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family.
Front Endocrinol (Lausanne)
0
2023
Author NameAffiliation
Iftikhar AhmedGomal University
Khalid A Fakhro
Khalid A FakhroWeill Cornell Medical College-Doha
Khalid A FakhroCollege of Health and Life Sciences, Hamad Bin Khalifa University
  • 1 - 4

Datasets

Release 1.2