Clinical and genetic studies for a cohort of patients with congenital stationary night blindness.

Authors:
Huang L; Bai X; Xie Y; Zhou Y; Wu J and 1 more

Journal:
Orphanet J Rare Dis

Publication Year: 2024

DOI:
10.1186/s13023-024-03091-3

PMCID:
PMC10918914

PMID:
38448886

Journal Information

Full Title: Orphanet J Rare Dis

Abbreviation: Orphanet J Rare Dis

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Medicine

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:

"Declarations Ethics approval and consent to participateThe human ethics committees at Beijing Children’s Hospital approved the protocol ([2022]-E-213-R). All protocols adhered to the tenets of the Declaration of Helsinki. All participants provided written informed consent. Consent for publicationWritten consent was obtained for all involved participants. Competing interestsThe authors have no proprietary or commercial interest in any materials discussed in this article. Competing interests The authors have no proprietary or commercial interest in any materials discussed in this article."

Evidence found in paper:

"Funding The study was supported by the National Natural Science Foundation of China (No.81670883), Fujian Provincial Health Technology Project (No.2023GGA047) and Natural Science Foundation of Fujian Province (No.2023J01724)."

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