Glycogen storage disease (Type IV): a familial cirrhosis diagnosed by electron microscopy (case report).

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dc.contributor.authorKalra, Ven_US
dc.contributor.authorArya, L Sen_US
dc.contributor.authorNayak, N Cen_US
dc.date.accessioned1980-07-01en_US
dc.date.accessioned2009-05-27T05:55:24Z
dc.date.available1980-07-01en_US
dc.date.available2009-05-27T05:55:24Z
dc.date.issued1980-07-01en_US
dc.identifier.citationKalra V, Arya LS, Nayak NC. Glycogen storage disease (Type IV): a familial cirrhosis diagnosed by electron microscopy (case report). Indian Pediatrics. 1980 Jul; 17(7): 625-7en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/13936
dc.language.isoengen_US
dc.source.urihttps://indianpediatrics.neten_US
dc.subject.meshGlycogen Storage Disease --diagnosisen_US
dc.subject.meshGlycogen Storage Disease Type IV --diagnosisen_US
dc.subject.meshHumansen_US
dc.subject.meshInfanten_US
dc.subject.meshLiver --ultrastructureen_US
dc.subject.meshLiver Cirrhosis --geneticsen_US
dc.subject.meshMaleen_US
dc.subject.meshMicroscopy, Electronen_US
dc.titleGlycogen storage disease (Type IV): a familial cirrhosis diagnosed by electron microscopy (case report).en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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