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Listar por Patrocinador "Crown Human Genome Center"

RiuNet: Repositorio Institucional de la Universidad Politécnica de Valencia

Listar por Patrocinador "Crown Human Genome Center"

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    USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses 
    Adato, Avital; Vreugde, Sarah; Joensuu, Tarja; Avidan, Nili; Hamalainen, Riikka; Belenkiy, Olga; Olender, Tsviya; Bonne-Tamir, Batsheva; Ben-Asher, Edna; Espinós-Armero, Carmen Ángeles; Millán, José M.; Lehesjoki, Anna-Elina; Flannery, John G.; Avraham, Karen B.; Pietrokovski, Shmuel; Sankila, Eeva-Marja; Beckmann, Jacques S.; Lancet, Doron (Nature Publishing Group, 2002-06)
    [EN] Usher syndrome type 3 (USH3) is an autosomal recessive disorder characterised by the association of post-lingual progressive hearing loss, progressive visual loss due to retinitis pigmentosa and variable presence of ...