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Hereditary tyrosinaemia. clinical, enzymatic, and pathological study of an infant with the acute form of the disease.

dc.contributor.authorCarson, N A
dc.contributor.authorBiggart, J D
dc.contributor.authorBittles, A H
dc.contributor.authorDonovan, D
dc.date.accessioned2018-08-24T08:24:20Z
dc.date.available2018-08-24T08:24:20Z
dc.date.issued1976-02-01
dc.identifier.citationCarson, N A; Biggart, J D; Bittles, A H; Donovan, D (1976). Hereditary tyrosinaemia. clinical, enzymatic, and pathological study of an infant with the acute form of the disease.. Archives of Disease in Childhood 51 (2), 106-113
dc.identifier.issn0003-9888,1468-2044
dc.identifier.urihttp://hdl.handle.net/10379/8948
dc.publisherBMJ
dc.relation.ispartofArchives of Disease in Childhood
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.titleHereditary tyrosinaemia. clinical, enzymatic, and pathological study of an infant with the acute form of the disease.
dc.typeArticle
dc.identifier.doi10.1136/adc.51.2.106
dc.local.publishedsourcehttp://adc.bmj.com/content/archdischild/51/2/106.full.pdf
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Attribution-NonCommercial-NoDerivs 3.0 Ireland
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Ireland