[Detection and characterization of the types of CYP21A1P/CYP21A2 and TNXA/TNXB fused genes by long-read sequencing among children with Steroid 21-hydroxylase deficiency].
Year: 2024
Type: other
Source: PubMed
Authors: Qingxian Fu, Zhen Li, Shiyi Xu, Lingling Du, Huishu E, Limei Guan
Institutions: Fujian Medical University, Shanghai Children's Medical Center
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4405249911