{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,31]],"date-time":"2025-10-31T13:47:30Z","timestamp":1761918450045},"reference-count":27,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2002,8,27]],"date-time":"2002-08-27T00:00:00Z","timestamp":1030406400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[2002,12,15]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Four patients from three families with the clinical features of DOOR syndrome (onycho\u2010osteodystrophy, dystrophic thumbs, sensorineural deafness, and increased urinary levels of 2\u2010oxoglutarate) are the subjects of this report. Our report deals with the autosomal recessive form of the disease, wherein the activity of 2\u2010oxoglutarate decarboxylase (E1<jats:sub>0<\/jats:sub>) in fibroblasts and white blood cells of the patients is decreased. The activity of E1<jats:sub>0<\/jats:sub> in all patients' fibroblasts and white blood cells was significantly lower compared to the controls. This study demonstrates for the first time that E1<jats:sub>0<\/jats:sub> deficiency is an important biochemical marker for the autosomal recessive form of DOOR syndrome. \u00a9 2002 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.b.10804","type":"journal-article","created":{"date-parts":[[2002,12,2]],"date-time":"2002-12-02T13:52:40Z","timestamp":1038837160000},"page":"371-374","source":"Crossref","is-referenced-by-count":18,"title":["DOOR syndrome: Deficiency of E1 component of the 2\u2010oxoglutarate dehydrogenase 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