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Title:	SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations
Source:	European Journal of Human Genetics [1018-4813] Albert, Sébastien yr:2006

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description	1.	Berrettini S, S. "Large vestibular aqueduct syndrome: audiological, radiological, clinical, and genetic features." American Journal of Otolaryngology 26.6 (2005): 363-71.
description	2.	Petersen, P J B. "Non-syndromic, autosomal-recessive deafness." Clinical genetics 69.5 (2006): 371-92.
description	3.	Pinto, José A A. "Enlarged vestibular aqueduct syndrome: report of 3 cases and literature review." Revista brasileira de oto-rino-laringologia (2005): 386-391.
description	4.	Bigozzi, M. "Pendred syndrome: study of three families." Acta otorhinolaryngologica Italica 25.4 (2005): 233-239.
description	5.	Markovich, D. "Pathogenetics of the human SLC26 transporters." Current medicinal chemistry 12.4 (2005): 385-396.
description	6.	Lin, Chun-Yu Y. "The remediation of hearing deterioration in children with large vestibular aqueduct syndrome." Auris, nasus, larynx 32.2 (2005): 99-105.
description	7.	Steinbach, S. "The large vestibular aqueduct – case report and review of the literature." Acta oto-laryngologica 126.8 (2006): 788-95.
description	8.	Mimura, T. "Hearing loss in patients with enlarged vestibular aqueduct: air-bone gap and audiological Bing test." International journal of audiology 44.8 (2005): 466-9.
description	9.	Ko, Shigeru B H H. "A molecular mechanism for aberrantCFTR-dependent HCO 3-transport in cystic fibrosis." The EMBO journal 21.21 (2002): 5662-5672.
description	10.	Veeriah, S. "Somatic mutations of the Parkinson's disease–associated gene PARK2 in glioblastoma and other human malignancies." Nature Genetics 42.1 (2010): 77-82.
description	11.	Bitner-Glindzicz, M. "Hereditary deafness and phenotyping in humans." British Medical Bulletin 63.1 (2002): 73-94.
description	12.	Yang, Jiann-Jou J. "Hearing loss associated with enlarged vestibular aqueduct and Mondini dysplasia is caused by splice-site mutation in the PDS gene." Hearing research 199.1-2 (2004): 22-30.
description	13.	Manzari, L. "Enlarged vestibular aqueduct (EVA) related with recurrent benign paroxysmal positional vertigo (BPPV)." Medical Hypotheses 70.1 (2008): 61-5.
description	14.	Madden, C. "Enlarged vestibular aqueduct syndrome in the pediatric population." Otology & neurotology 24.4 (2003): 625-32.
description	15.	Rotteveel, Liselotte J C J. "Cochlear implantation in 53 patients with otosclerosis: demographics, computed tomographic scanning, surgery, and complications." Otology & neurotology 26.4 (2004): 943-52.
description	16.	Koesling, S. "Imaging and clinical findings in large endolymphatic duct and sac syndrome." European journal of radiology 57.1 (2005): 54-62.
description	17.	Shannon, Robert V. "Understanding hearing through deafness." Proceedings of the National Academy of Sciences of the United States of America 104.17 (2007): 6883-6884.
description	18.	Pandya A, A. "Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands." Genetics in medicine 5.4 (2003): 295-303.
description	19.	Zhao HB, T W W. "Gap junctions and cochlear homeostasis." The Journal of membrane biology 209.2-3 (2006): 177-86.
description	20.	Jayaram, M M M. "Prevalence and audiological characteristics in individuals with auditory neuropathy/auditory dys-synchrony." International journal of audiology 45.6 (2006): 360-6.