High carrier frequency of a nonsense p.Trp230* variant in HSD3B2 gene in Ossetians.

Saved in:
Bibliographic Details
Title: High carrier frequency of a nonsense p.Trp230* variant in HSD3B2 gene in Ossetians.
Authors: Makretskaya N; Department of Genetics of Endocrine Diseases, Research Centre for Medical Genetics, Moscow, Russia., Kalinchenko N; Institute of Pediatric Endocrinology, Endocrinology Research Centre, Moscow, Russia., Tebieva I; Consulting and Diagnostic Department, Republic of North Ossetia-Alania (RNOA) 'Republican Children's Clinical Hospital', Vladikavkaz, Russia., Ionova S; Department of Genetics of Endocrine Diseases, Research Centre for Medical Genetics, Moscow, Russia., Zinchenko R; Department of Genetics of Endocrine Diseases, Research Centre for Medical Genetics, Moscow, Russia., Marakhonov A; Department of Genetics of Endocrine Diseases, Research Centre for Medical Genetics, Moscow, Russia., Tiulpakov A; Department of Genetics of Endocrine Diseases, Research Centre for Medical Genetics, Moscow, Russia.
Source: Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2023 May 16; Vol. 14, pp. 1146768. Date of Electronic Publication: 2023 May 16 (Print Publication: 2023).
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2392 (Print) Linking ISSN: 16642392 NLM ISO Abbreviation: Front Endocrinol (Lausanne) Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1664-2392
DOI:10.3389/fendo.2023.1146768