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TWO ADOLESCENT PATIENTS WITH RIBOFLAVIN RESPONSIVE MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY (RR-MADD): A RARE DISORDER WITH HETEROGENEOUS CLINICAL FINDINGS

dc.contributor.authorAydın, Ali Fuat
dc.contributor.authorCEYLANER, S.
dc.contributor.authorCansever, M. S.
dc.contributor.authorAltay, Serdar
dc.contributor.authorAktuglu Zeybek, A. C.
dc.contributor.authorKiykim, Ertuğrul
dc.date.accessioned2021-03-05T21:24:11Z
dc.date.available2021-03-05T21:24:11Z
dc.identifier.citationAktuglu Zeybek A. C. , Kiykim E., Cansever M. S. , CEYLANER S., Altay S., Aydın A. F. , "TWO ADOLESCENT PATIENTS WITH RIBOFLAVIN RESPONSIVE MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY (RR-MADD): A RARE DISORDER WITH HETEROGENEOUS CLINICAL FINDINGS", JOURNAL OF INHERITED METABOLIC DISEASE, cilt.35, 2012
dc.identifier.issn0141-8955
dc.identifier.othervv_1032021
dc.identifier.otherav_d8ba5009-c997-4283-99a0-e0178d1f34cc
dc.identifier.urihttp://hdl.handle.net/20.500.12627/142989
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectTıbbi Genetik
dc.subjectTıbbi Ekoloji ve Hidroklimatoloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTIP, ARAŞTIRMA VE DENEYSEL
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.titleTWO ADOLESCENT PATIENTS WITH RIBOFLAVIN RESPONSIVE MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY (RR-MADD): A RARE DISORDER WITH HETEROGENEOUS CLINICAL FINDINGS
dc.typeMakale
dc.relation.journalJOURNAL OF INHERITED METABOLIC DISEASE
dc.contributor.departmentIntergen Genetic Diseases Diagnosis Center , ,
dc.identifier.volume35
dc.contributor.firstauthorID80762


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