Compound Heterozygote of a Novel Missense Mutation (p. K402T) and a Double Missense Mutation (p.[G71R;Y486D]) in Type II Crigler-Najjar Syndrome

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dc.contributor.authorMaruo, Yoshihiro
dc.contributor.authorOzgenc, Funda
dc.contributor.authorMimura, Yu
dc.contributor.authorOta, Yoriko
dc.contributor.authorMatsui, Katsuyuki
dc.contributor.authorTakahashi, Hiroko
dc.contributor.authorMori, Asami
dc.contributor.authorTaga, Takashi
dc.contributor.authorTakano, Tomoyuki
dc.contributor.authorSato, Hiroshi
dc.contributor.authorTakeuchi, Yoshihiro
dc.date.accessioned2019-10-27T21:24:51Z
dc.date.available2019-10-27T21:24:51Z
dc.date.issued2011
dc.departmentEge Üniversitesien_US
dc.identifier.doi10.1097/MPG.0b013e3181fcafb8en_US
dc.identifier.endpage365en_US
dc.identifier.issn0277-2116
dc.identifier.issue3en_US
dc.identifier.pmid21297505en_US
dc.identifier.startpage362en_US
dc.identifier.urihttps://doi.org/10.1097/MPG.0b013e3181fcafb8
dc.identifier.urihttps://hdl.handle.net/11454/44681
dc.identifier.volume52en_US
dc.identifier.wosWOS:000287477100019en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.ispartofJournal of Pediatric Gastroenterology and Nutritionen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleCompound Heterozygote of a Novel Missense Mutation (p. K402T) and a Double Missense Mutation (p.[G71R;Y486D]) in Type II Crigler-Najjar Syndromeen_US
dc.typeArticleen_US

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