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

Detalles Bibliográficos
Autores principales:	Gupta, Neerja, Verma, Gaurav, Kabra, Madhulika, Bijarnia-Mahay, Sunita, Ganapathy, Aparna
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2018
Materias:	Correspondence
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057243/ https://www.ncbi.nlm.nih.gov/pubmed/29998879 http://dx.doi.org/10.4103/ijmr.IJMR_820_16

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