identification of a case of srd5a3-congenital disorder of glycosylation (cdg1q) by exome sequencing
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identification of a case of srd5a3-congenital disorder of glycosylation (cdg1q) by exome sequencing

;Neerja Gupta;Gaurav Verma;Madhulika Kabra;Sunita Bijarnia-Mahay;Aparna Ganapathy
international journal of radiation biology 2018 Vol. 147 pp. 422-426
168
gupta2018indianidentification

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Medicine

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DOI:
10.4103/ijmr.IJMR_820_16
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http://www.ijmr.org.in/article.asp?issn=0971-5916;...

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