{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,2,10]],"date-time":"2024-02-10T00:29:49Z","timestamp":1707524989535},"reference-count":8,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2023,4,17]]},"DOI":"10.7759\/cureus.37719","type":"journal-article","created":{"date-parts":[[2023,4,17]],"date-time":"2023-04-17T19:24:13Z","timestamp":1681759453000},"source":"Crossref","is-referenced-by-count":0,"title":["Retinitis Pigmentosa Sine Pigmento in a Carrier of Usher Syndrome"],"prefix":"10.7759","author":[{"given":"Sof\u00eda C","family":"Ayala Rodr\u00edguez","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Estefania","family":"Ramirez Marquez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrea","family":"Robles Bocanegra","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Natalio","family":"Izquierdo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Armando L","family":"Oliver","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1159\/000322473","article-title":"Usher syndrome: hearing loss with vision loss","volume":"70","author":"Friedman TB","year":"2011","unstructured":"Friedman TB, Schultz JM, Ahmed ZM, Tsilou ET, Brewer CC. Usher syndrome: hearing loss with vision loss. Adv Otorhinolaryngol. 2011, 70:56-65. 10.1159\/000322473","journal-title":"Adv Otorhinolaryngol"},{"key":"ref2","article-title":"Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis","volume":"22","author":"Ben-Rebeh I","year":"2016","unstructured":"Ben-Rebeh I, Grati M, Bonnet C, et al.. Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis. Mol Vis. 2016, 22:827-35.","journal-title":"Mol Vis"},{"key":"ref3","article-title":"A rare type of Usher's syndrome","volume":"52","author":"Antonela GA","year":"2013","unstructured":"Antonela GA, Snje\u017eana K, Kajo B, Mira I, Maja R, Ksenija K. A rare type of Usher's syndrome. Acta Clin Croat. 2013, 52:506-15.","journal-title":"Acta Clin Croat"},{"key":"ref4","article-title":"Usher's syndrome--case report","volume":"110","author":"Kwiecie\u0144 S","year":"2008","unstructured":"Kwiecie\u0144 S, Sulak R, Szaflik J. Usher's syndrome--case report. Klin Oczna. 2008, 110:384-6.","journal-title":"Klin Oczna"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1186\/1750-1172-1-40","article-title":"Retinitis pigmentosa","volume":"1","author":"Hamel C","year":"2006","unstructured":"Hamel C. Retinitis pigmentosa. Orphanet J Rare Dis. 2006, 1:40. 10.1186\/1750-1172-1-40","journal-title":"Orphanet J Rare Dis"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1080\/01658107.2017.1292532","article-title":"Retinitis pigmentosa sine pigmento mimicking a chiasm disease","volume":"41","author":"Pellegrini F","year":"2017","unstructured":"Pellegrini F, Prosdocimo G, Romano F, Interlandi E. Retinitis pigmentosa sine pigmento mimicking a chiasm disease. Neuroophthalmology. 2017, 41:198-201. 10.1080\/01658107.2017.1292532","journal-title":"Neuroophthalmology"},{"key":"ref7","article-title":"Novel mutations in the USH1C gene in Usher syndrome patients","volume":"16","author":"Aparisi MJ","year":"2010","unstructured":"Aparisi MJ, Garc\u00eda-Garc\u00eda G, Jaijo T, et al.. Novel mutations in the USH1C gene in Usher syndrome patients. Mol Vis. 2010, 16:2948-54.","journal-title":"Mol Vis"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1016\/j.neuron.2009.04.006","article-title":"Harmonin mutations cause mechanotransduction defects in cochlear hair cells","volume":"62","author":"Grillet N","year":"2009","unstructured":"Grillet N, Xiong W, Reynolds A, et al.. Harmonin mutations cause mechanotransduction defects in cochlear hair cells. Neuron. 2009, 62:375-87. 10.1016\/j.neuron.2009.04.006","journal-title":"Neuron"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/137134-retinitis-pigmentosa-sine-pigmento-in-a-carrier-of-usher-syndrome","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T19:59:48Z","timestamp":1707508788000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/137134-retinitis-pigmentosa-sine-pigmento-in-a-carrier-of-usher-syndrome"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,4,17]]},"references-count":8,"URL":"https:\/\/doi.org\/10.7759\/cureus.37719","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2023,4,17]]}}}