Accession PRJCA003969
Title The common molecular mechanism exploration of microtia and congenital sensorineural hearing loss by samples sequencing and bioinformatics approach
Relevance Medical
Data types Exome
Targeted Locus (Loci)
Organisms Homo sapiens
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.
Sample scope Multiisolate
Release date 2020-12-02
Publication
PubMed ID Article title Journal name DOI Year
35000142 The genes for sensory perception of sound should be considered in gene diagnosis of congenital sensorineural hearing loss and microtia Journal of Applied Genetics 10.1007/s13353-021-00674-9 2022
Data provider
Data provider Data provider URL
Lin Ken https://www.med-credit.org.cn/hospital/show/1293.html
Grants
Agency program Grant ID Grant title
Kunming Medical University 2019FE001-275 Yunnan Applied Basic Research-Joint Special Project
Submitter LIN    KEN  (526823761@qq.com)
Organization The Affiliated Hospital of Kunming Medical University
Submission date 2020-12-02

Project Data

Resource name Description
BioSample (14)  show -