Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41436-018-0142-1
Title: Correction to: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders (Genetics in Medicine, (2018), 10.1038/s41436-018-0008-6)
Authors: Bylstra Y.
Kuan J.L.
Lim W.K.
Bhalshankar J.D.
Teo J.X.
Davila S.
Teh B.T.
Rozen S.
Tan E.-C.
Liew W.K.M.
Yeo K.K.
Tan P.
Saw S.M. 
Cheng C.-Y. 
Cook S.
Foo R. 
Jamuar S.S.
The SinGapore Incidental Finding (SGIF) study group
Issue Date: 2018
Publisher: Nature Publishing Group
Citation: Bylstra Y., Kuan J.L., Lim W.K., Bhalshankar J.D., Teo J.X., Davila S., Teh B.T., Rozen S., Tan E.-C., Liew W.K.M., Yeo K.K., Tan P., Saw S.M., Cheng C.-Y., Cook S., Foo R., Jamuar S.S., The SinGapore Incidental Finding (SGIF) study group (2018). Correction to: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders (Genetics in Medicine, (2018), 10.1038/s41436-018-0008-6). Genetics in Medicine. ScholarBank@NUS Repository. https://doi.org/10.1038/s41436-018-0142-1
Abstract: At the time of publication the author Jyn Ling Kuan did not have a master's degree; this has now been amended to BSc. This has now been corrected in the PDF and HTML versions of the article. © 2018, American College of Medical Genetics and Genomics.
Source Title: Genetics in Medicine
URI: http://scholarbank.nus.edu.sg/handle/10635/152050
ISSN: 10983600
DOI: 10.1038/s41436-018-0142-1
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