{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,24]],"date-time":"2025-10-24T13:05:55Z","timestamp":1761311155925},"reference-count":19,"publisher":"Cambridge University Press (CUP)","issue":"3","license":[{"start":{"date-parts":[[2014,8,1]],"date-time":"2014-08-01T00:00:00Z","timestamp":1406851200000},"content-version":"unspecified","delay-in-days":18659,"URL":"https:\/\/www.cambridge.org\/core\/terms"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Acta genet. med. gemellol."],"published-print":{"date-parts":[[1963,7]]},"abstract":"<jats:title>SUMMARY<\/jats:title><jats:p>A family of Iranian-Jewish origin with two hereditary enzymatic defects in the red blood cells, catalase deficiency and glucose-6-phosphate dehydrogenase deficiency, is described. The two enzymatic defects were inherited independently of each other. The findings are compatible with a transmission of the catalase deficiency by an autosomal gene of incomplete dominance, the homozygous state resulting in severe catalase deficiency and the heterozygous state in intermediate catalase deficiency.<\/jats:p>","DOI":"10.1017\/s1120962300016231","type":"journal-article","created":{"date-parts":[[2016,7,27]],"date-time":"2016-07-27T09:46:07Z","timestamp":1469612767000},"page":"247-255","source":"Crossref","is-referenced-by-count":10,"title":["A dual hereditary red blood cell defect in one family: Hypocatalasemia and glucose-6-phosphate dehydrogenase deficiency"],"prefix":"10.1017","volume":"12","author":[{"given":"\u00c0.","family":"Szeinberg","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"\u00c0.","family":"de Vries","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Pinkhas","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Djaldetti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Ezra","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"56","published-online":{"date-parts":[[2014,8,1]]},"reference":[{"key":"S1120962300016231_ref007","first-page":"323","volume-title":"Glucose-6-phosphate dehydrogenase in Methods of Enzymology","volume":"I","author":"Kornberg","year":"1955"},{"key":"S1120962300016231_ref013","doi-asserted-by":"crossref","first-page":"603","DOI":"10.1182\/blood.V12.7.603.603","article-title":"Studies on erythrocytes in cases with past history of favism and drug induced acute hemolytic anemia","volume":"12","author":"Szeinberg","year":"1957","journal-title":"Blood"},{"key":"S1120962300016231_ref001","doi-asserted-by":"publisher","DOI":"10.1007\/BF02158293"},{"key":"S1120962300016231_ref010","first-page":"333","article-title":"Immunologic evidence of catalase deficiency in human hereditary acatalasemia","volume":"10","author":"Nishimura","year":"1961","journal-title":"Laboratory Invest."},{"key":"S1120962300016231_ref017","first-page":"204","volume-title":"J. 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Lab. Clin. Med."},{"key":"S1120962300016231_ref005","first-page":"21","article-title":"A genetic study of a defect in glutathione metabolism of the erythrocyte","volume":"102","author":"Childs","year":"1958","journal-title":"Bull. Johns Hopkins Hosp."},{"key":"S1120962300016231_ref002","first-page":"469","article-title":"A specific enzymatic assay for diagnosis of congenital galactosemia. I. The consumption test","volume":"50","author":"Anderson","year":"1957","journal-title":"J. Clin. Invest."},{"key":"S1120962300016231_ref009","unstructured":"Motulsky A. : 1960. Personal communication."},{"key":"S1120962300016231_ref016","doi-asserted-by":"publisher","DOI":"10.1172\/JCI104075"},{"key":"S1120962300016231_ref003","first-page":"286","article-title":"The hemolytic effect of primaquine. VII. Biochemical studies of drug sensitive erythrocytes","volume":"45","author":"Beutler","year":"1955","journal-title":"J. Lab. Clin. 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Wochensch."},{"key":"S1120962300016231_ref015","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(52)90939-2"},{"key":"S1120962300016231_ref006","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(61)91476-3"},{"key":"S1120962300016231_ref014","doi-asserted-by":"crossref","first-page":"1043","DOI":"10.1182\/blood.V13.11.1043.1043","article-title":"Selective occurrence of glutathione instability in red blood corpuscles of the various Jewish tribes","volume":"13","author":"Szeinberg","year":"1958","journal-title":"Blood"}],"container-title":["Acta geneticae medicae et gemellologiae"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cambridge.org\/core\/services\/aop-cambridge-core\/content\/view\/S1120962300016231","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,24]],"date-time":"2020-09-24T11:11:42Z","timestamp":1600945902000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cambridge.org\/core\/product\/identifier\/S1120962300016231\/type\/journal_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1963,7]]},"references-count":19,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1963,7]]}},"alternative-id":["S1120962300016231"],"URL":"https:\/\/doi.org\/10.1017\/s1120962300016231","relation":{},"ISSN":["1120-9623","2059-6316"],"issn-type":[{"value":"1120-9623","type":"print"},{"value":"2059-6316","type":"electronic"}],"subject":[],"published":{"date-parts":[[1963,7]]}}}