APA (7th ed.) Citation

Nejati, P., Falsafi, N., Alimoradi, E., Khosravi, T., Kamari, M., Oladnabi, M., & Alibakhshi, R. (2025). A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy. BMC Medical Genomics, 18(1), 1. https://doi.org/10.1186/s12920-025-02254-w

Chicago Style (17th ed.) Citation

Nejati, Parham, Nafiseh Falsafi, Elham Alimoradi, Teymoor Khosravi, Mohana Kamari, Morteza Oladnabi, and Reza Alibakhshi. "A Novel Compound Heterozygous Variant in LAMA2 Gene in a Family with Merosin-deficient Congenital Muscular Dystrophy." BMC Medical Genomics 18, no. 1 (2025): 1. https://doi.org/10.1186/s12920-025-02254-w.

MLA (9th ed.) Citation

Nejati, Parham, et al. "A Novel Compound Heterozygous Variant in LAMA2 Gene in a Family with Merosin-deficient Congenital Muscular Dystrophy." BMC Medical Genomics, vol. 18, no. 1, 2025, p. 1, https://doi.org/10.1186/s12920-025-02254-w.