https://boris-portal.unibe.ch/entities/publication/2aac8fb6-f747-45a8-9f46-66cef94caa50
A novel GH-1 gene mutation (GH-P59L) causes partial GH deficiency type II combined with bioinactive...
Despite the differences in the main characteristics between the autosomal dominant form of GH deficiency (IGHD II) and the bioinactive GH syndrome, a common...