The common molecular mechanism exploration of microtia by samples sequencing and bioinformatics approach.
Release date:
2022-12-01
Description:
Numerous independent researches of congenital sensorineural hearing loss (CSHL) or microtia have been performed. In contrast, the common molecular mechanism has not been reported, although some cases with both phenotypes of CSHL and microtia have been observed in previous researches.Our objective is to identify the common molecular mechanism of CSHL and microtia.
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Numerous independent researches of congenital sensorineural hearing loss or microtia have been performed. In contrast, the common molecular mechanism has not been reported, although some cases with both phenotypes of CSHL and microtia have been observed in previous researches.Our objective is to identify the common molecular mechanism of CSHL and microtia.
Organization: Kunming Institute of Zoology, Chinese Academy of Sciences
Submission date: 2020-12-02
Requests: -
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HRA000485.xlsx