Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families

Autor: Di Leva, F., Adamo Pio d'Adamo, Strollo, L., Auletta, G., Caravelli, A., Carella, M., Mari, F., Livi, W., Renieri, A., Gasparini, P., D Urso, M., Marciano, E., Franzé, A.

Publikováno v: Università degli Studi di Siena-IRIS
Scopus-Elsevier
International journal of audiology (Online) 42 (2003): 475–480. doi:10.3109/14992020309081517
info:cnr-pdr/source/autori:Di Leva F, D'Adamo AP, Strollo L, Auletta G, Caravelli A, Carella M, Mari F, Livi W, Renieri A, Gasparini P, D'Urso M, Marciano E, Franze A./titolo:Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families./doi:10.3109%2F14992020309081517/rivista:International journal of audiology (Online)/anno:2003/pagina_da:475/pagina_a:480/intervallo_pagine:475–480/volume:42

Otosclerosis is the single most common cause of hearing impairment among adult caucasians. Little is known about its aetiology and its molecular aspects. Until now, genetic linkage in otosclerosis has been demonstrated in an Indian family and a Belgi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::afced0be3a1c3a756a32c675aee8030c
http://hdl.handle.net/11365/3734

Otosclerosi:analisi di associazione cromosomica e identificazione di geni candidati

Autor: AULETTA G., CARAVELLI A, CARRABBA L, CARELLA M, D’ ADAMO P, DI LEVA F, FRANZE', Annamaria, GASPARINI P, SEQUINO L, STROLLO L, D’ URSO M, MARCIANO, ELIO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3730::d5b138c5685501085aa33718fd95f010
http://hdl.handle.net/11588/187807

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