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HARVARD Citation
Ge, L. et al. (2018). Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy. Scientific reports. 8 (1), pp. 1-10. [Online].
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Ge, L. et al. (2018). Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy. Scientific reports. 8 (1), pp. 1-10. [Online].