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Are heterocygotes for classical homocystinuria at risk of vitamin B-12 and folic acid deficiency?

dc.contributor.authorABDOH, Ghassan
dc.contributor.authorBener, Abdulbari
dc.contributor.authorHOFFMANN, Georg F.
dc.contributor.authorZSCHOCKE, Johannes
dc.contributor.authorBESSISSO, Mohammed S.
dc.contributor.authorELSAID, Mahmoud F.
dc.contributor.authorLINDNER, Martin
dc.contributor.authorALZYOUD, Mahmoud
dc.contributor.authorSHAHBEK, Noora
dc.contributor.authorABDELRAHMAN, Mohammed O.
dc.date.accessioned2021-03-04T11:51:53Z
dc.date.available2021-03-04T11:51:53Z
dc.identifier.citationELSAID M. F. , Bener A., LINDNER M., ALZYOUD M., SHAHBEK N., ABDELRAHMAN M. O. , ABDOH G., BESSISSO M. S. , ZSCHOCKE J., HOFFMANN G. F. , "Are heterocygotes for classical homocystinuria at risk of vitamin B-12 and folic acid deficiency?", MOLECULAR GENETICS AND METABOLISM, cilt.92, ss.100-103, 2007
dc.identifier.issn1096-7192
dc.identifier.otherav_747f3d40-5385-4973-89c0-0784933a7e92
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/80070
dc.identifier.urihttps://doi.org/10.1016/j.ymgme.2007.06.010
dc.description.abstractObjectives/design: Comparative cross-sectional study to assess homocysteine and vitamin status in carriers of CBS gene mutations.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectTıbbi Genetik
dc.subjectTıbbi Ekoloji ve Hidroklimatoloji
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
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.titleAre heterocygotes for classical homocystinuria at risk of vitamin B-12 and folic acid deficiency?
dc.typeMakale
dc.relation.journalMOLECULAR GENETICS AND METABOLISM
dc.contributor.department, ,
dc.identifier.volume92
dc.identifier.startpage100
dc.identifier.endpage103
dc.contributor.firstauthorID96019


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