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Identification of a case of SRD5A3-congenital disorder of glycosylation (CDG1Q) by exome sequencing.

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Title: Identification of a case of SRD5A3-congenital disorder of glycosylation (CDG1Q) by exome sequencing.
Authors: Gupta, Neerja1 neerja17aiims@gmail.com, Verma, Gaurav1, Kabra, Madhulika1, Bijarnia-Mahay, Sunita2, Ganapathy, Aparna3
Source: Indian Journal of Medical Research. Apr2018, Vol. 147 Issue 4, p422-426. 5p.
Database: Academic Search Ultimate
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  Data: Identification of a case of SRD5A3-congenital disorder of glycosylation (CDG1Q) by exome sequencing.
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  Data: <searchLink fieldCode="AR" term="%22Gupta%2C+Neerja%22">Gupta, Neerja</searchLink><relatesTo>1</relatesTo><i> neerja17aiims@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Verma%2C+Gaurav%22">Verma, Gaurav</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Kabra%2C+Madhulika%22">Kabra, Madhulika</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Bijarnia-Mahay%2C+Sunita%22">Bijarnia-Mahay, Sunita</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Ganapathy%2C+Aparna%22">Ganapathy, Aparna</searchLink><relatesTo>3</relatesTo>
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  Data: <searchLink fieldCode="JN" term="%22Indian+Journal+of+Medical+Research%22">Indian Journal of Medical Research</searchLink>. Apr2018, Vol. 147 Issue 4, p422-426. 5p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=130622119
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        Value: 10.4103/ijmr.IJMR_820_16
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        Text: English
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      – TitleFull: Identification of a case of SRD5A3-congenital disorder of glycosylation (CDG1Q) by exome sequencing.
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              Text: Apr2018
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              Y: 2018
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