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Article

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

The Indian journal of medical research - 1 Apr 2018

Gupta Neerja, Verma Gaurav, Kabra Madhulika, Bijarnia-Mahay Sunita, Ganapathy Aparna

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Share to Congenital Disorders of Glycosylation
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 29998879
DOI: 10.4103/ijmr.IJMR_820_16
PMCID: PMC6057243

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