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Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation.

Zhao HM, Yang YJ, Duan JQ, Ouyang HJ, Liu L, Yi LC, Xiao ZH, Zheng Y, Peng L, Attard TM, Li DY, You JY. Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation. J Pediatr Gastroenterol Nutr. 2019 02; 68(2):199-206.

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