{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,2]],"date-time":"2025-10-02T00:29:34Z","timestamp":1759364974480,"version":"build-2065373602"},"reference-count":18,"publisher":"Elsevier BV","issue":"6","license":[{"start":{"date-parts":[[2016,11,1]],"date-time":"2016-11-01T00:00:00Z","timestamp":1477958400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2016,11,1]],"date-time":"2016-11-01T00:00:00Z","timestamp":1477958400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"name":"Intramural Research Program","award":["Z99 CL999999"],"award-info":[{"award-number":["Z99 CL999999"]}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["American Journal of Otolaryngology"],"published-print":{"date-parts":[[2016,11]]},"DOI":"10.1016\/j.amjoto.2015.07.006","type":"journal-article","created":{"date-parts":[[2015,7,16]],"date-time":"2015-07-16T11:15:21Z","timestamp":1437045321000},"page":"484-489","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"title":["A genetic marker of the ACKR1 gene is present in patients with Type II congenital smell loss who have type I hyposmia and hypogeusia"],"prefix":"10.1016","volume":"37","author":[{"given":"William A.","family":"Stateman","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2504-7350","authenticated-orcid":false,"given":"Alexandra B.","family":"Kn\u00f6ppel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Willy A.","family":"Flegel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Robert I.","family":"Henkin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.amjoto.2015.07.006_bb0005","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1097\/00004728-200201000-00008","article-title":"Functional MRI of congenital hyposmia: brain activation to odors and imagination of odors and tastes","volume":"26","author":"Henkin","year":"2002","journal-title":"J Comput Assist Tomogr"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0010","first-page":"203","article-title":"The genetic aspects of primary eunuchoidism","volume":"48","author":"Kallmann","year":"1944","journal-title":"Am J Ment Defic"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0015","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1016\/j.amjoto.2013.04.006","article-title":"Taste and smell function in chronic disease: a review of clinical and biochemical evaluations of taste and smell dysfunction in over 5000 patients at The Taste and Smell Clinic in Washington, DC","volume":"34","author":"Henkin","year":"2013","journal-title":"Am J Otolaryngol"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0020","doi-asserted-by":"crossref","first-page":"457","DOI":"10.1172\/JCI29884","article-title":"Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism","volume":"117","author":"Pitteloud","year":"2007","journal-title":"J Clin Invest"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0025","doi-asserted-by":"crossref","first-page":"138","DOI":"10.1016\/j.mce.2013.02.016","article-title":"The genetic basis of female reproductive disorders: etiology and clinical testing","volume":"370","author":"Layman","year":"2013","journal-title":"Mol Cell Endocrinol"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0030","doi-asserted-by":"crossref","first-page":"1424","DOI":"10.1016\/j.fertnstert.2011.09.046","article-title":"The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome","volume":"96","author":"Quaynor","year":"2011","journal-title":"Fertil Steril"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0035","doi-asserted-by":"crossref","first-page":"1831","DOI":"10.1016\/j.fertnstert.2013.01.149","article-title":"Identification of HESX1 mutations in Kallmann syndrome","volume":"99","author":"Newbern","year":"2013","journal-title":"Fertil Steril"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0040","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1093\/chemse\/bjl032","article-title":"Mutations in olfactory signal transduction genes are not a major cause of human congenital general anosmia","volume":"32","author":"Feldmesser","year":"2007","journal-title":"Chem Senses"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0045","doi-asserted-by":"crossref","first-page":"146","DOI":"10.1016\/j.amjoto.2014.10.006","article-title":"Erythrocyte membrane antigen frequencies in patients with Type II congenital smell loss","volume":"36","author":"Stateman","year":"2015","journal-title":"Am J Otolaryngol"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0050","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1124\/pr.113.007724","article-title":"International Union of Basic and Clinical Pharmacology. [corrected]. LXXXIX. Update on the extended family of chemokine receptors and introducing a new nomenclature for atypical chemokine receptors","volume":"66","author":"Bacheleri","year":"2013","journal-title":"Pharmacol Rev"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0055","doi-asserted-by":"crossref","first-page":"650","DOI":"10.1097\/RCT.0b013e31829bfa3b","article-title":"Anatomic olfactory structural abnormalities in congenital smell loss: magnetic resonance imaging evaluation of olfactory bulb, groove, sulcal and hippocampal morphology","volume":"37","author":"Levy","year":"2013","journal-title":"J Comput Assist Tomogr"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0060","first-page":"28","article-title":"Applying molecular immunohaematology to regularly transfused thalassaemic patients in Thailand","volume":"12","author":"Rujirojindakul","year":"2014","journal-title":"Blood Transfus"},{"year":"2012","series-title":"The blood group antigen factsbook","author":"Reid","key":"10.1016\/j.amjoto.2015.07.006_bb0065"},{"year":"2005","series-title":"Blood groups and red cell antigens","author":"Dean","key":"10.1016\/j.amjoto.2015.07.006_bb0070"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0075","first-page":"65","article-title":"A simple sequentially rejective multiple test procedure","volume":"6","author":"Holm","year":"1979","journal-title":"Scand J Stat"},{"author":"NCBI","key":"10.1016\/j.amjoto.2015.07.006_bb0080"},{"author":"NCBI","key":"10.1016\/j.amjoto.2015.07.006_bb0085"},{"key":"10.1016\/j.amjoto.2015.07.006_bb0090","series-title":"Olfaction and taste II","first-page":"235","article-title":"The definition of primary and accessory areas of olfaction as the basis for a classification of decreased olfactory acuity","author":"Henkin","year":"1967"}],"container-title":["American Journal of Otolaryngology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0196070915001404?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0196070915001404?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,1]],"date-time":"2025-10-01T04:59:47Z","timestamp":1759294787000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0196070915001404"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,11]]},"references-count":18,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2016,11]]}},"alternative-id":["S0196070915001404"],"URL":"https:\/\/doi.org\/10.1016\/j.amjoto.2015.07.006","relation":{},"ISSN":["0196-0709"],"issn-type":[{"type":"print","value":"0196-0709"}],"subject":[],"published":{"date-parts":[[2016,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"A genetic marker of the ACKR1 gene is present in patients with Type II congenital smell loss who have type I hyposmia and hypogeusia","name":"articletitle","label":"Article Title"},{"value":"American Journal of Otolaryngology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.amjoto.2015.07.006","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2015 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}