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

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Bibliographic Details
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

Description
ISSN:	09715916
DOI:	10.4103/ijmr.IJMR_820_16