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HARVARD Citation
Zhao, Z. et al. (2018). A novel mutation (c.855delG) in STK11 gene is associated with Peutz–Jeghers syndrome in a Chinese family. Digestive and liver disease. 50 (3), pp. 312-314. [Online].
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Zhao, Z. et al. (2018). A novel mutation (c.855delG) in STK11 gene is associated with Peutz–Jeghers syndrome in a Chinese family. Digestive and liver disease. 50 (3), pp. 312-314. [Online].