Diagnosing CAH-X syndrome by long-read sequencing and identifying a novel genotype
Zhen Li1, Shiyi Xu1, Qingxian Fu1
1Department of Endocrinology and Inborn Metabolic Diseases, Fujian Children's Hospital (Fujian Branch of Shanghai Children's Medical Center); College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, 350014, China.
Orphanet Journal of Rare Diseases
|April 23, 2026
Abstract
No abstract available in PubMed .
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