The Genotype-Phenotype Correlation İn Phenylketonuria Patients With P.L48s Mutation

Simple item page
dc.contributor.authorUslu Gizem
dc.contributor.authorBalcı Mehmet Cihan
dc.contributor.authorMuslu Mücahit
dc.contributor.authorGedikbaşı Asuman
dc.contributor.authorGökçay Gülden Fatma
dc.contributor.authorDemirkol Mübeccel
dc.date.accessioned2024-03-22T20:37:01Z
dc.date.available2024-03-22T20:37:01Z
dc.date.issued2019
dc.identifier.doi10.1002/jimd.12153
dc.identifier.endpage479
dc.identifier.isbn0141-8955
dc.identifier.issn1573-2665
dc.identifier.issueS1
dc.identifier.startpage1
dc.identifier.urihttp://wileyonlinelibrary.com/journal/jimd
dc.identifier.urihttps://hdl.handle.net/20.500.12597/28179
dc.identifier.volume42
dc.languageEnglish
dc.relation.conferenceSsıem 2019: Annual Symposium Of The Society For Thestudy Of Inborn Errors Of Metabolism, Rotterdam,The Netherlands, 3–6 September 2019
dc.relation.conferencecityRotterdam
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.titleThe Genotype-Phenotype Correlation İn Phenylketonuria Patients With P.L48s Mutation
dc.typeConference Proceedings
local.event.enddate06.09.2019
local.event.printdate25.08.2019
local.event.startdate03.09.2019
local.import.id5793866-4374416
local.item.editiontypeBasılı+Elektronik
local.item.presentationstylePoster
local.item.scopeUluslararası
local.item.subjectSağlık Bilimleri Temel Alanı->Çocuk Metabolizma Hastalıkları
local.item.typeÖzet Bildiri
local.item.yayinID5793866
local.item.yazarID4374416
local.person.branchSağlık Bilimleri Fakültesi
person.jobTitleÖğretim Görevlisi

Files

Collections

Bildiriler