Genetic screening of 15 hearing loss variants in 77,647 neonates with clinical follow-up.

Publication Year: 2023

DOI:
10.1002/mgg3.2324

PMCID:
PMC10767602

PMID:
38037722

Journal Information

Full Title: Mol Genet Genomic Med

Abbreviation: Mol Genet Genomic Med

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Genetics, Medical

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

Transparency Score
3/6
50.0% Transparent
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Evidence found in paper:

"CONFLICT OF INTEREST STATEMENT The authors agree on the publication of the study and declare that they have no competing interests or personal relationships that might influence the work reported in this study."

Evidence found in paper:

"FUNDING INFORMATION This work was financially supported by Key Project on Science and Technology Program of Fujian Health Commission (grant number 2021ZD01002), Putian Public Health Foundation Project (2019–2021)."

Protocol Registration
Open Access
Paper is freely available to read
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Assessment Info

Tool: rtransparent

OST Version: N/A

Last Updated: Aug 05, 2025