Investigation of Fibrillar Aggregates Formed by Pathogenic Pre-pro-vasopressin Mutants that Cause ADNDI
RD Vaizoglu, B Erdem, M Gul, C Acar… - The Journal of …, 2024 - academic.oup.com
Context Aggregations of unfolded or misfolded proteins, both inside and outside cells, are
implicated in numerous diseases, collectively known as amyloidosis. Particularly, autosomal …
implicated in numerous diseases, collectively known as amyloidosis. Particularly, autosomal …
[HTML][HTML] Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel nonsense mutation in AVP‑NPII gene
H Yang, K Yan, L Wang, F Gong… - Experimental and …, 2019 - spandidos-publications.com
Familial neurohypophyseal diabetes insipidus (FNDI) is a rare single‑gene disorder caused
by mutations of the arginine vasopressin‑neurophysin II (AVP‑NPII) gene. These changes …
by mutations of the arginine vasopressin‑neurophysin II (AVP‑NPII) gene. These changes …