{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,11,21]],"date-time":"2023-11-21T00:58:38Z","timestamp":1700528318583},"reference-count":13,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1977,1,1]],"date-time":"1977-01-01T00:00:00Z","timestamp":220924800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hum Genet"],"published-print":{"date-parts":[[1977]]},"DOI":"10.1007\/bf00295431","type":"journal-article","created":{"date-parts":[[2004,11,9]],"date-time":"2004-11-09T17:51:48Z","timestamp":1100022708000},"page":"353-357","source":"Crossref","is-referenced-by-count":1,"title":["?Gd(-) H\ufffdtel Dieu?: A new G-6PD variant with chronic hemolysis in a Negro patient from Senegal"],"prefix":"10.1007","volume":"39","author":[{"given":"Axel","family":"Kahn","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christian","family":"Dao","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dominique","family":"Cottreau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Georges","family":"Bilski-Pasquier","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"1005","DOI":"10.1016\/S0022-3476(72)80014-3","volume":"80","author":"E. Beutler","year":"1972","unstructured":"Beutler, E., Grooms, A. M., Morgan, S. K., Trinidad, F.: Chronic severe hemolytic anemia due to G.6PD Charleston: A new deficient variant. J. Pediatr. 80, 1005?1009 (1972)","journal-title":"J. Pediatr."},{"key":"CR2","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1111\/j.1469-1809.1973.tb01823.x","volume":"37","author":"E. Beutler","year":"1973","unstructured":"Beutler, E., Yoshida, A.: Human glucose-6-phosphate dehydrogenase variants: A supplementary tabulation. Ann. Hum. Genet. 37, 151?155 (1973)","journal-title":"Ann. Hum. Genet."},{"key":"CR3","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1016\/S0022-3476(77)80774-9","volume":"90","author":"R. Feldman","year":"1977","unstructured":"Feldman, R., Gromisch, D. S., Luhby, A. L., Beutler, E.: Congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase East Harlem: A new deficient variant. J. Pediatr. 90, 89?91 (1977)","journal-title":"J. Pediatr."},{"key":"CR4","doi-asserted-by":"crossref","first-page":"624","DOI":"10.1542\/peds.37.4.624","volume":"37","author":"A. Grossman","year":"1966","unstructured":"Grossman, A., Ramanathan, K., Justice, P., Gordon, J., Shahidi, N. T., Hsia, D.: Congenital nonspherocytic hemolytic anemia associated with erythrocyte G-6PD deficiency in a Negro family. Pediatrics 37, 624?629 (1966)","journal-title":"Pediatrics"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"160","DOI":"10.1136\/jmg.9.2.160","volume":"9","author":"E. B. Howell","year":"1972","unstructured":"Howell, E. B., Nelson, A. J., Jones, O. W.: A new G.6PD variant associated with chronic nonspherocytic haemolytic anaemia in a Negro family. J. Med. Genet. 9, 160?164 (1972)","journal-title":"J. Med. Genet."},{"key":"CR6","first-page":"741","volume":"11","author":"A. Kahn","year":"1971","unstructured":"Kahn, A., Boivin, P., Hakim, J., Lagneau, J.: Heterog\ufffdn\ufffdit\ufffd des glucose-6-phosphate d\ufffdshydrog\ufffdnases \ufffdrythrocytaires d\ufffdficitaires dans la race noire. \ufffdtude cin\ufffdtique et description de deux nouvelles variantes, Gd(-) Dakar et Gd(-) Mali. Nouv. Rev. Fr. Hematol. 11, 741?758 (1971)","journal-title":"Nouv. Rev. Fr. Hematol."},{"key":"CR7","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1007\/BF00290606","volume":"18","author":"A. Kahn","year":"1973","unstructured":"Kahn, A., Boivin, P., Lagneau, J.: Ph\ufffdnotypes de la glucose-6-phosphate d\ufffdshydrog\ufffdnase \ufffdrythrocytaire dans la race noire. \ufffdtude de 301 noirs vivant en France et description de 9 variantes diff\ufffdrentes. Fr\ufffdquence \ufffdlev\ufffde d'une enzyme d\ufffdficitaire de migration \ufffdB\ufffd. Hum. Genet. 18, 261?270 (1973)","journal-title":"Hum. Genet."},{"key":"CR8","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1007\/BF00283310","volume":"25","author":"A. Kahn","year":"1974","unstructured":"Kahn, A., Cottreau, D., Boivin, P.: Molecular mechanisms of glucose-6-phosphate dehydrogenase deficiency. Hum. Genet. 25, 101?109 (1974)","journal-title":"Hum. Genet."},{"key":"CR9","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1016\/0009-8981(75)90027-3","volume":"59","author":"A. Kahn","year":"1975","unstructured":"Kahn, A., Hakim, J., Cottreau, D., Boivin, P.: Gd(-) Matam, an african G.6PD variant with enzyme deficiency. Biochemical and immunological properties in various hemopoietic tissues. Clin. Chim. Acta 59, 183?190 (1975)","journal-title":"Clin. Chim. Acta"},{"key":"CR10","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1007\/BF00291500","volume":"33","author":"A. Kahn","year":"1976","unstructured":"Kahn, A., Esters, A., Habedank, M.: Gd(-) Aachen, a new variant of deficient glucose-6-phosphate dehydrogenase. Clinical genetic and biological aspects. Hum. Genet. 33, 171?180 (1976)","journal-title":"Hum. Genet."},{"key":"CR11","first-page":"1","volume":"366","author":"WHO","year":"1967","unstructured":"WHO: Standardization of procedures for the study of glucose-6-phosphate dehydrogenase. WHO Tech. Rep. Ser. 366, 1 (1967)","journal-title":"WHO Tech. Rep. Ser."},{"key":"CR12","first-page":"243","volume":"45","author":"A. Yoshida","year":"1971","unstructured":"Yoshida, A., Beutler, E., Motulsky, A.G.: Table of human glucose-6-phosphate dehydrogenase variants. Bull. WHO 45, 243?253 (1971)","journal-title":"Bull. WHO"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"532","DOI":"10.1126\/science.179.4073.532","volume":"179","author":"A. Yoshida","year":"1973","unstructured":"Yoshida, A.: Hemolytic anemia and G.6PD deficiency. Science 179, 532?537 (1973)","journal-title":"Science"}],"container-title":["Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00295431.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00295431\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00295431","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,4,30]],"date-time":"2023-04-30T03:03:11Z","timestamp":1682823791000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00295431"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1977]]},"references-count":13,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1977]]}},"alternative-id":["BF00295431"],"URL":"https:\/\/doi.org\/10.1007\/bf00295431","relation":{},"ISSN":["0340-6717","1432-1203"],"issn-type":[{"value":"0340-6717","type":"print"},{"value":"1432-1203","type":"electronic"}],"subject":[],"published":{"date-parts":[[1977]]}}}