Trio-Based Whole-Exome Sequencing Identifies a De novo EFNB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay

  • Ji Yoon Han
  • , Hyun Jeong Kim
  • , Ja Hyun Jang
  • , In Goo Lee
  • , Joonhong Park

Research output: Contribution to journal › Article › peer-review

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Biochemistry, Genetics and Molecular Biology