{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T16:31:01Z","timestamp":1786120261150,"version":"build-2736575974"},"reference-count":0,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2012,1]]},"DOI":"10.1097\/mcd.0b013e32834af585","type":"journal-article","created":{"date-parts":[[2011,10,4]],"date-time":"2011-10-04T19:07:36Z","timestamp":1317755256000},"page":"1-7","source":"Crossref","is-referenced-by-count":1,"title":["A newly described mutation of the CLCN7 gene causes neuropathic autosomal recessive osteopetrosis in an Arab family"],"prefix":"10.1097","volume":"21","author":[{"given":"Jumana Y.","family":"Al-Aama","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amal A.","family":"Dabbagh","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alaa Y.","family":"Edrees","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","container-title":["Clinical Dysmorphology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/00019605-201201000-00001","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,6]],"date-time":"2026-08-06T20:23:31Z","timestamp":1786047811000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/00019605-201201000-00001"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,1]]},"references-count":0,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2012]]}},"URL":"https:\/\/doi.org\/10.1097\/mcd.0b013e32834af585","relation":{},"ISSN":["0962-8827"],"issn-type":[{"value":"0962-8827","type":"print"}],"subject":[],"published":{"date-parts":[[2012,1]]}}}