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Article

Rare Mutations in AHDC1 in Patients with Obstructive Sleep Apnea.

BioMed research international - 1 Jan 2019

Yang Song, Li Kun, Zhu Miao-Miao, Yuan Xian-Dao, Jiao Xiao-Lu, Yang Yun-Yun, Li Juan, Li Linyi, Zhang Hui-Na, Du Yun-Hui, Wei Yong-Xiang, Qin Yan-Wen

Abstract excerpt

OBJECTIVES: Obstructive sleep apnea (OSA) is a common disorder influenced by genetic and environmental factors. Mutations of AT-hook DNA-binding motif containing 1 (AHDC1) gene have been implicated which could cause rare syndromes presenting OSA. This study aims to investigate some rare mutations of AHDC1 in Chinese Han individuals with OSA. PATIENTS AND METHODS: Three hundred and seventy-five patients with OSA...

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Identifiers

PMID: 31737670
DOI: 10.1155/2019/5907361
PMCID: PMC6815587

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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