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L-2-Hydroxyglutaric Aciduria: Report of Four Turkish Patients from the Same Family

dc.contributor.authorYalcin, A. Destina
dc.contributor.authorTekturk, Pinar
dc.contributor.authorYapici, Zuhal
dc.date.accessioned2021-03-04T14:43:12Z
dc.date.available2021-03-04T14:43:12Z
dc.date.issued2016
dc.identifier.citationYalcin A. D. , Tekturk P., Yapici Z., "L-2-Hydroxyglutaric Aciduria: Report of Four Turkish Patients from the Same Family", JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH, cilt.33, sa.3, ss.494-500, 2016
dc.identifier.issn1302-1664
dc.identifier.othervv_1032021
dc.identifier.otherav_8300ba9e-7e90-4d29-b6e3-77ef68d38943
dc.identifier.urihttp://hdl.handle.net/20.500.12627/89196
dc.description.abstractBackground: L-2-Hydroxyglutaric aciduria is a rare slow progressive autosomal recessively inherited neurometabolic disease.
dc.language.isoeng
dc.subjectSinirbilim ve Davranış
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri
dc.subjectNEUROSCIENCES
dc.subjectYaşam Bilimleri (LIFE)
dc.titleL-2-Hydroxyglutaric Aciduria: Report of Four Turkish Patients from the Same Family
dc.typeMakale
dc.relation.journalJOURNAL OF NEUROLOGICAL SCIENCES-TURKISH
dc.contributor.departmentIstanbul Umraniye Training & Research Hospital , ,
dc.identifier.volume33
dc.identifier.issue3
dc.identifier.startpage494
dc.identifier.endpage500
dc.contributor.firstauthorID227785


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