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Article

Prevalence of A1555G mitochondrial mutation in Chinese newborns and the correlation with neonatal hearing screening.

International journal of pediatric otorhinolaryngology - 1 Apr 2011

Chen Guanming, Wang Xiyin, Fu Siqing

Abstract excerpt

OBJECTIVE: To investigate the feasibility of genetic screening for deafness causative genes in the process of newborn hearing screening in China. METHODS: Total 865 newborn babies between November 2009 and March 2010 were enrolled for the simultaneous hearing and deafness causative gene screening in Tongji Hospital, Wuhan, China. Hearing screening followed a two-stage strategy with transient evoked otoacoustic...

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PMID: 21324532
DOI: 10.1016/j.ijporl.2011.01.013

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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