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OCTN2 GENE MUTATIONS IN TURKISH PATIENTS WITH PRIMARY CARNITINE DEFICIENCY

dc.contributor.authorDursun, A.
dc.contributor.authorBalci, Mehmet Cihan
dc.contributor.authorKilic, M.
dc.contributor.authorOzgul, R. K.
dc.contributor.authorErsoy, M.
dc.contributor.authorGokcay, G.
dc.contributor.authorYucel-Yilmaz, D.
dc.contributor.authorCandan, S.
dc.date.accessioned2021-03-03T20:09:22Z
dc.date.available2021-03-03T20:09:22Z
dc.identifier.citationYucel-Yilmaz D., Ersoy M., Candan S., Balci M. C. , Kilic M., Gokcay G., Dursun A., Ozgul R. K. , "OCTN2 GENE MUTATIONS IN TURKISH PATIENTS WITH PRIMARY CARNITINE DEFICIENCY", JOURNAL OF INHERITED METABOLIC DISEASE, cilt.35, 2012
dc.identifier.issn0141-8955
dc.identifier.othervv_1032021
dc.identifier.otherav_586910bc-cdb5-4b03-aafd-42a407899070
dc.identifier.urihttp://hdl.handle.net/20.500.12627/62263
dc.language.isoeng
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectTIP, ARAŞTIRMA VE DENEYSEL
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectTıbbi Ekoloji ve Hidroklimatoloji
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectYaşam Bilimleri (LIFE)
dc.titleOCTN2 GENE MUTATIONS IN TURKISH PATIENTS WITH PRIMARY CARNITINE DEFICIENCY
dc.typeMakale
dc.relation.journalJOURNAL OF INHERITED METABOLIC DISEASE
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume35
dc.contributor.firstauthorID205831


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