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Rare Mutations in AHDC1 in Patients with Obstructive Sleep Apnea
2019
BioMed Research International
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 and one hundred and nine control individuals underwent polysomnography. A targeted
doi:10.1155/2019/5907361
pmid:31737670
pmcid:PMC6815587
fatcat:chkvakbqcjdhrh33wqwrjwr5am