{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,27]],"date-time":"2025-10-27T16:13:06Z","timestamp":1761581586420,"version":"build-2065373602"},"reference-count":8,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2017,7,1]],"date-time":"2017-07-01T00:00:00Z","timestamp":1498867200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2017,7,1]],"date-time":"2017-07-01T00:00:00Z","timestamp":1498867200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/501100001411","name":"Indian Council of Medical Research","doi-asserted-by":"publisher","award":["Tribal\/64\/2012-ECD-II"],"award-info":[{"award-number":["Tribal\/64\/2012-ECD-II"]}],"id":[{"id":"10.13039\/501100001411","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Blood Cells, Molecules, and Diseases"],"published-print":{"date-parts":[[2017,7]]},"DOI":"10.1016\/j.bcmd.2017.07.002","type":"journal-article","created":{"date-parts":[[2017,7,20]],"date-time":"2017-07-20T13:17:29Z","timestamp":1500556649000},"page":"8-10","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"special_numbering":"C","title":["Does novel P5\u2032N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?"],"prefix":"10.1016","volume":"66","author":[{"given":"Prashant","family":"Warang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rati","family":"Devendra","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ashish","family":"Chiddarwar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vinod","family":"Gupta","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Darshana","family":"Mirgal","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anshul","family":"Jadli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aniket","family":"Mohite","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Prabhakar","family":"Kedar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Malay","family":"Mukherjee","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.bcmd.2017.07.002_bb0005","series-title":"Red Cell Metabolism: A Manual of Biochemical Methods","first-page":"1","author":"Beutler","year":"1984"},{"key":"10.1016\/j.bcmd.2017.07.002_bb0010","doi-asserted-by":"crossref","first-page":"74","DOI":"10.1182\/asheducation-2007.1.74","article-title":"Coagulation in the pathophysiology of hemolytic anemia","author":"Cappellini","year":"2007","journal-title":"Hematology Am. Soc. Hematol. Educ. Program"},{"key":"10.1016\/j.bcmd.2017.07.002_bb0015","doi-asserted-by":"crossref","first-page":"1481","DOI":"10.3324\/haematol.2009.013672","article-title":"Hypercoagulability and thrombotic complications in hemolytic anemias","volume":"94","author":"Ataga","year":"2009","journal-title":"Haematologica"},{"key":"10.1016\/j.bcmd.2017.07.002_bb0020","doi-asserted-by":"crossref","first-page":"365","DOI":"10.3389\/fphys.2013.00365","article-title":"Red blood cell vesiculation in hereditary hemolytic anemia","volume":"4","author":"Alaarg","year":"2013","journal-title":"Front. Physiol."},{"key":"10.1016\/j.bcmd.2017.07.002_bb0025","doi-asserted-by":"crossref","first-page":"696","DOI":"10.1016\/j.jhep.2009.06.019","article-title":"Paroxysmal nocturnal hemoglobinuria in Budd-Chiari syndrome: findings from a cohort study","volume":"51","author":"Hoekstra","year":"2009","journal-title":"J. Hepatol."},{"key":"10.1016\/j.bcmd.2017.07.002_bb0030","doi-asserted-by":"crossref","first-page":"1021","DOI":"10.1053\/jhep.2001.24114","article-title":"Sickle cell hepatopathy","volume":"33","author":"Banerjee","year":"2003","journal-title":"Hepatology"},{"key":"10.1016\/j.bcmd.2017.07.002_bb0035","doi-asserted-by":"crossref","first-page":"1498","DOI":"10.1182\/blood.V99.4.1498","article-title":"A single mutation 202G>A in the human glucose-6-phosphate dehydrogenase gene (G6PD) can cause acute hemolysis by itself","volume":"99","author":"Hirono","year":"2001","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2017.07.002_bb0040","doi-asserted-by":"crossref","first-page":"715","DOI":"10.1007\/s00277-012-1616-x","article-title":"New missense homozygous mutation (Q270Ter) in the pyrimidine 5\u2032 nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia","volume":"92","author":"Warang","year":"2013","journal-title":"Ann. Hematol."}],"container-title":["Blood Cells, Molecules, and Diseases"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S107997961730219X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S107997961730219X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T12:32:21Z","timestamp":1761049941000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S107997961730219X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,7]]},"references-count":8,"alternative-id":["S107997961730219X"],"URL":"https:\/\/doi.org\/10.1016\/j.bcmd.2017.07.002","relation":{},"ISSN":["1079-9796"],"issn-type":[{"type":"print","value":"1079-9796"}],"subject":[],"published":{"date-parts":[[2017,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Does novel P5\u2032N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?","name":"articletitle","label":"Article Title"},{"value":"Blood Cells, Molecules, and Diseases","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.bcmd.2017.07.002","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}