Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients.

Authors:
Lin F; Yang K; Lin X; Jin M; Chen L and 7 more

Journal:
Orphanet J Rare Dis

Publication Year: 2023

DOI:
10.1186/s13023-023-02897-x

PMCID:
PMC10652577

PMID:
37974208

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 participateAll procedures in studies involving human participants were performed in accordance with the ethical standards of the institutional committee and/or national research committee (The First Affiliated Hospital of Fujian Medical University FYYY2006-01-19-01) and with the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards. Informed consent Informed consent was obtained from all individual participants included in the study. Consent for publicationNot applicable. Competing interestsAll authors declare that they have no competing interests. Competing interests All authors declare that they have no competing interests."

Evidence found in paper:

"Funding This study was supported by grants from the National Natural Science Foundation of China (81701242, Beijing); the Joint Fund for Program of Science Innovation of Fujian Province, China (2018Y9079); and the National Natural Science Foundation of Fujian Province, China (2023J01620)."

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Last Updated: Aug 05, 2025