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HARVARD Citation
Song, D. et al. (2020). A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients. Clinical genetics. 97 (5), pp. 789-790. [Online].
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Song, D. et al. (2020). A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients. Clinical genetics. 97 (5), pp. 789-790. [Online].