{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,27]],"date-time":"2025-10-27T04:48:18Z","timestamp":1761540498259},"reference-count":11,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2004,3,11]],"date-time":"2004-03-11T00:00:00Z","timestamp":1078963200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Haemophilia"],"published-print":{"date-parts":[[2004,5]]},"abstract":"<jats:p><jats:bold>Summary.\u2002<\/jats:bold> When excluding haemophilia and von Willebrand disease, coagulation factors deficiencies constitute rare autosomal recessive disorders (&lt;1 in 500\u2003000) of less precisely defined epidemiology. We have reported herein the distribution of these entities in the French Basque Country, a genetic isolate of very old individualization with peculiar biological specificities. The prevalence of these disorders was markedly high, especially, as already shown, factor XI deficiency. This unusual profile needs to be discussed in the view of population genetics.<\/jats:p>","DOI":"10.1111\/j.1365-2516.2004.00892.x","type":"journal-article","created":{"date-parts":[[2004,4,14]],"date-time":"2004-04-14T13:17:38Z","timestamp":1081948658000},"page":"276-279","source":"Crossref","is-referenced-by-count":7,"title":["Is there a \u2018Basque\u2019 profile regarding autosomal recessive deficiencies of coagulation factors?*"],"prefix":"10.1111","volume":"10","author":[{"given":"F.","family":"Bauduer","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Ducout","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"O.","family":"Dutour","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Degioanni","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2004,3,11]]},"reference":[{"key":"e_1_2_8_2_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1468-0734.2001.00051.x"},{"key":"e_1_2_8_3_2","volume-title":"The History and Geography of Human Genes","author":"Cavalli\u2010Sforza LL","year":"1994"},{"key":"e_1_2_8_4_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.2002.00699.x"},{"key":"e_1_2_8_5_2","first-page":"S83","article-title":"Molecular and clinical aspects of factor VII deficiency","volume":"9","author":"Mariani G","year":"1998","journal-title":"Blood Coagul Fibrinolysis"},{"key":"e_1_2_8_6_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.2002.00659.x"},{"key":"e_1_2_8_7_2","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1055\/s-0038-1642386","article-title":"The prevalence of moderate and severe FXII (Hageman factor) deficiency among the normal population: evaluation of the incidence of FXII deficiency among 300 healthy blood donors","volume":"71","author":"Halbmayer WM","year":"1994","journal-title":"Thromb Haemost"},{"key":"e_1_2_8_8_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0268-960X(95)90027-6"},{"key":"e_1_2_8_9_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.1999.00316.x"},{"key":"e_1_2_8_10_2","doi-asserted-by":"publisher","DOI":"10.1182\/blood.V99.7.2448"},{"key":"e_1_2_8_11_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.1998.440677.x"},{"key":"e_1_2_8_12_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.2000.00421.x"}],"container-title":["Haemophilia"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fj.1365-2516.2004.00892.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/j.1365-2516.2004.00892.x","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,13]],"date-time":"2023-10-13T05:47:07Z","timestamp":1697176027000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/j.1365-2516.2004.00892.x"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2004,3,11]]},"references-count":11,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2004,5]]}},"alternative-id":["10.1111\/j.1365-2516.2004.00892.x"],"URL":"https:\/\/doi.org\/10.1111\/j.1365-2516.2004.00892.x","archive":["Portico"],"relation":{},"ISSN":["1351-8216","1365-2516"],"issn-type":[{"value":"1351-8216","type":"print"},{"value":"1365-2516","type":"electronic"}],"subject":[],"published":{"date-parts":[[2004,3,11]]}}}