Genitopatellar Syndrome Secondary to De Novo KAT6B Mutation: The First Genetically Confirmed Case in South Korea-Reference-Cited by-同舟云学术

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Genitopatellar Syndrome Secondary to De Novo KAT6B Mutation: The First Genetically Confirmed Case in South Korea

Published:2019 Issue:4 Volume:60 Page:395
ISSN:0513-5796
Container-title:Yonsei Medical Journal
language:en
Short-container-title:Yonsei Med J

Author:

Kim Byuh Ree¹^ORCID,Han Jeong Ho²^ORCID,Shin Jeong Eun²^ORCID,Park Min Soo²^ORCID,Park Kook In²^ORCID,Namgung Ran²^ORCID,Lee Hyun-Joo³^ORCID,Lee Jin-Sung³^ORCID,Eun Ho Sun²^ORCID

Affiliation:

1. Department of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, Korea.

2. Division of Neonatology, Department of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, Korea.

3. Division of Clinical Genetics, Department of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, Korea.

Publisher

Yonsei University College of Medicine

Subject

General Medicine

Link

https://synapse.koreamed.org/pdf/10.3349/ymj.2019.60.4.395

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A neonate with Say–Barber–Biesecker–Young–Simpson syndrome with a novel pathogenic mutation in KAT6B gene: A case report;Journal of Genetic Medicine;2021-12-31

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