{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,11,21]],"date-time":"2023-11-21T00:59:22Z","timestamp":1700528362176},"reference-count":12,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2006,7,11]],"date-time":"2006-07-11T00:00:00Z","timestamp":1152576000000},"content-version":"vor","delay-in-days":9841,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J Hematol"],"published-print":{"date-parts":[[1979,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Glucose 6\u2010phosphate dehydrogenase (G\u20106\u2010PD) deficiency was identified in three children who were evaluated because of chronic nonspherocytic hemolytic anemia. One child is of German extraction, another Puerto Rican, and the third Mexican. In each of the patients the hemolytic process was well compensated, but each had one or more episodes of anemia following exposure to an oxidant drug or with infections. The electrophoretic, functional, and kinetic properties of the mutant enzymes, derived both from the patients' erythrocytes and from cultured fibroblasts, allowed each to be distinguished from G\u20106\u2010PD variants previously described.<\/jats:p>","DOI":"10.1002\/ajh.2830060407","type":"journal-article","created":{"date-parts":[[2007,2,21]],"date-time":"2007-02-21T05:22:47Z","timestamp":1172035367000},"page":"353-360","source":"Crossref","is-referenced-by-count":6,"title":["Three new variants of glucose\u20106\u2010phosphate dehydrogenase associated with chronic nonspherocytic hemolytic anemia: G\u20106\u2010PD Lincoln Park, G\u20106\u2010PD arlington heights, and G\u20106\u2010PD West Town"],"prefix":"10.1002","volume":"6","author":[{"given":"George R.","family":"Honig","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Evelina","family":"Habacon","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Loyda N.","family":"Vida","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Florinda","family":"Matsumoto","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ernest","family":"Beutler","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2006,7,11]]},"reference":[{"key":"e_1_2_1_2_2","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1182\/blood.V31.2.131.131","article-title":"Biochemical variants of glucose\u20106\u2010phosphate dehydiogenase giving rise to congenital nonspherocytic hemolytic disease","volume":"31","author":"Beutler E","year":"1968","journal-title":"Blood"},{"key":"e_1_2_1_3_2","unstructured":"BetkeK BrewerGJ KirkmanHN LuzzatoL MotulskyAG RamotB SiniscalcoM BeutlerE StandleyCC: Standardization of procedures for the study of glucose\u20106\u2010phosphate dehydrogenase. 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