Identification and functional characterization of a novel heterozygous splice‑site mutation in the calpain 3 gene causes rare autosomal dominant limb‑girdle muscular dystrophy.
Journal Information
Full Title: Exp Ther Med
Abbreviation: Exp Ther Med
Country: Unknown
Publisher: Unknown
Language: N/A
Publication Details
Subject Category: Medicine, Research & Experimental
Available in Europe PMC: Yes
Available in PMC: Yes
PDF Available: No
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"Competing interests The authors declare that they have no competing interests."
"Funding: This study is supported by the Key Research and Development Plan of Gansu Province (grant no. 21YF1FA115), Key Research and Development Plan of Gansu Province in 2022 (grant no. 22YF7FA084) and Natural Science Foundation of Gansu Province in 2022 (grant no. 22JR5RA911)."
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Last Updated: Aug 05, 2025