dc.contributor.author | Mitchell, G. | |
dc.contributor.author | Mubeccel, D. | |
dc.contributor.author | Erol, I | |
dc.contributor.author | Matthijs, G. | |
dc.contributor.author | Jaeken, J. | |
dc.contributor.author | Gokcay, G. | |
dc.contributor.author | Rymen, D. | |
dc.contributor.author | Rymen, D. | |
dc.contributor.author | Keldermans, L. | |
dc.contributor.author | Quelhas, D. | |
dc.contributor.author | Snyder, F. F. | |
dc.contributor.author | Alehan, F. | |
dc.date.accessioned | 2021-03-03T07:39:06Z | |
dc.date.available | 2021-03-03T07:39:06Z | |
dc.identifier.citation | Rymen D., Rymen D., Keldermans L., Quelhas D., Snyder F. F. , Alehan F., Erol I., Mubeccel D., Gokcay G., Mitchell G., et al., "SRD5A3-CDG: AN IMPORTANT GROUP OF DOLICHOL-PHOSPHATE SYNTHESIS DEFECTS", JOURNAL OF INHERITED METABOLIC DISEASE, cilt.35, 2012 | |
dc.identifier.issn | 0141-8955 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_1317594b-cf7a-4848-8b72-b21451809b54 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/18289 | |
dc.language.iso | eng | |
dc.subject | ENDOKRİNOLOJİ VE METABOLİZMA | |
dc.subject | TIP, ARAŞTIRMA VE DENEYSEL | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | İç Hastalıkları | |
dc.subject | Endokrinoloji ve Metabolizma Hastalıkları | |
dc.subject | Tıbbi Genetik | |
dc.subject | Tıbbi Ekoloji ve Hidroklimatoloji | |
dc.subject | Yaşam Bilimleri | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Temel Bilimler | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | GENETİK VE HAYAT | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.title | SRD5A3-CDG: AN IMPORTANT GROUP OF DOLICHOL-PHOSPHATE SYNTHESIS DEFECTS | |
dc.type | Makale | |
dc.relation.journal | JOURNAL OF INHERITED METABOLIC DISEASE | |
dc.contributor.department | İstanbul Üniversitesi , , | |
dc.identifier.volume | 35 | |
dc.contributor.firstauthorID | 206021 | |