High clinical utility of long-read sequencing for precise diagnosis of congenital adrenal hyperplasia in 322 probands
Abstract Background The molecular genetic diagnosis of congenital adrenal hyperplasia (CAH) is very challenging due to the high homology between the CYP21A2 gene and its pseudogene CYP21A1P. Methodology This study aims to assess the clinical efficacy of targeted long-read sequencing (T-LRS) by compa...
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Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2025-01-01
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Series: | Human Genomics |
Subjects: | |
Online Access: | https://doi.org/10.1186/s40246-024-00696-4 |
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