Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders-Reference-Cited by-同舟云学术

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Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders

Published:2019-01 Issue:1 Volume:21 Page:207-212
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Bylstra Yasmin,Kuan Jyn Ling,Lim Weng Khong,Bhalshankar Jaydutt Digambar,Teo Jing Xian,Davila Sonia,Te Teh Bin an,Rozen Steve,Tan Ene-Choo,Liew Wendy Kein Meng,Yeo Khung Keong,Tan Patrick,Saw Seang Mei,Cheng Ching-Yu,Cook Stuart,Foo Roger,Jamuar Saumya Shekhar

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

https://www.nature.com/articles/s41436-018-0008-6.pdf

Reference26 articles.

Cited by 21 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. Investigating common mutations in ATP7B gene and the prevalence of Wilson’s disease in the Thai population using population-based genome-wide datasets;Journal of Human Genetics;2024-08-28

2. Citrin deficiency—The East‐side story;Journal of Inherited Metabolic Disease;2024-07-12

3. Clinical landscape of citrin deficiency: A global perspective on a multifaceted condition;Journal of Inherited Metabolic Disease;2024-03-19

4. Changing the standardised obstetric care by expanded carrier screening and counselling: a multicentre prospective cohort study;Journal of Medical Genetics;2023-10-05

5. Genomic Sequencing as a First-Tier Screening Test and Outcomes of Newborn Screening;JAMA Network Open;2023-09-01

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