4.3 Article

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

Journal

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MPG.0000000000002166

Keywords

children; de novo mutation; hereditary cancer; Peutz-Jeghers syndrome; polyposis syndrome; STK11

Funding

  1. Health and Family Planning Commission Fund of Hunan Province [B2016040]
  2. national natural Science Foundation of china [31501017]
  3. Key laboratory fund of Hunan Province [2018tP1028]

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