{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,4,4]],"date-time":"2025-04-04T17:40:06Z","timestamp":1743788406320,"version":"3.40.3"},"reference-count":2,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[2000,12,1]],"date-time":"2000-12-01T00:00:00Z","timestamp":975628800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"},{"start":{"date-parts":[[2000,12,1]],"date-time":"2000-12-01T00:00:00Z","timestamp":975628800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Nat Rev Genet"],"published-print":{"date-parts":[[2000,12,1]]},"DOI":"10.1038\/35042025","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T08:48:04Z","timestamp":1027673284000},"page":"167-167","source":"Crossref","is-referenced-by-count":0,"title":["New light on night blindness"],"prefix":"10.1038","volume":"1","author":[{"given":"Jane","family":"Alfred","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF35042025_CR1","doi-asserted-by":"publisher","first-page":"319","DOI":"10.1038\/81619","volume":"26","author":"NT Bech-Hansen","year":"2000","unstructured":"Bech-Hansen N. T. et al. Mutations in  NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. Nature Genet.  26, 319\u2013323 (2000)","journal-title":"Nature Genet."},{"key":"BF35042025_CR2","doi-asserted-by":"publisher","first-page":"324","DOI":"10.1038\/81627","volume":"26","author":"CM Pusch","year":"2000","unstructured":"Pusch, C. M.  et al. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich protein . Nature Genet. 26, 324\u2013 327 (2000)","journal-title":"Nature Genet."}],"container-title":["Nature Reviews Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.nature.com\/articles\/35042025.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/35042025","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/35042025.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,4,4]],"date-time":"2025-04-04T17:07:55Z","timestamp":1743786475000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/35042025"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,12,1]]},"references-count":2,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2000,12,1]]}},"alternative-id":["BF35042025"],"URL":"https:\/\/doi.org\/10.1038\/35042025","relation":{},"ISSN":["1471-0056","1471-0064"],"issn-type":[{"type":"print","value":"1471-0056"},{"type":"electronic","value":"1471-0064"}],"subject":[],"published":{"date-parts":[[2000,12,1]]}}}